Artigo Acesso aberto Revisado por pares

Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients

1995; Wiley; Volume: 6; Issue: 3 Linguagem: Inglês

10.1002/humu.1380060314

ISSN

1098-1004

Autores

Ryoko Koike, Osamu Onodera, Hiroyuki Tabe, Kiyotoshi Kaneko, Tadashi Miyatake, Shinichi Iwasaki, Misa Nakano, Nami Shizuma, Kunihiko Ikeguchi, Masatoyo Nishizawa, Jean Mosser, Claude‐Olivier Sarde, Shoji Tsuji,

Tópico(s)

Microbial metabolism and enzyme function

Resumo

Human MutationVolume 6, Issue 3 p. 263-267 Mutation in Brief Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients Ryoko Koike, Corresponding Author Ryoko Koike Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanDepartment of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorOsamu Onodera, Osamu Onodera Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this authorHiroyuki Tabe, Hiroyuki Tabe Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this authorKiyotoshi Kaneko, Kiyotoshi Kaneko Department of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorTadashi Miyatake, Tadashi Miyatake Department of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorShinichi Iwasaki, Shinichi Iwasaki Department of Neurology, Saitama Medical School, Saitama, JapanSearch for more papers by this authorMisa Nakano, Misa Nakano Department of Neurology, Osaka University, Osaka, Japan Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorNami Shizuma, Nami Shizuma Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorKunihiko Ikeguchi, Kunihiko Ikeguchi Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorMasatoyo Nishizawa, Masatoyo Nishizawa Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorJean Mosser, Jean Mosser Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, INSERM Unité 184, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, FranceSearch for more papers by this authorClaude-Olivier Sarde, Claude-Olivier Sarde Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, INSERM Unité 184, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, FranceSearch for more papers by this authorShoji Tsuji, Shoji Tsuji Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this author Ryoko Koike, Corresponding Author Ryoko Koike Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanDepartment of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorOsamu Onodera, Osamu Onodera Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this authorHiroyuki Tabe, Hiroyuki Tabe Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this authorKiyotoshi Kaneko, Kiyotoshi Kaneko Department of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorTadashi Miyatake, Tadashi Miyatake Department of Neurology, Tokyo Medical and Dental University, Tokyo, JapanSearch for more papers by this authorShinichi Iwasaki, Shinichi Iwasaki Department of Neurology, Saitama Medical School, Saitama, JapanSearch for more papers by this authorMisa Nakano, Misa Nakano Department of Neurology, Osaka University, Osaka, Japan Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorNami Shizuma, Nami Shizuma Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorKunihiko Ikeguchi, Kunihiko Ikeguchi Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorMasatoyo Nishizawa, Masatoyo Nishizawa Department of Neurology, Jichi Medical School, Tochigi, JapanSearch for more papers by this authorJean Mosser, Jean Mosser Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, INSERM Unité 184, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, FranceSearch for more papers by this authorClaude-Olivier Sarde, Claude-Olivier Sarde Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, INSERM Unité 184, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, FranceSearch for more papers by this authorShoji Tsuji, Shoji Tsuji Department of Neurology, Brain Research Institute, Niigata University, 1-757 Asahimachi Niigata, JapanSearch for more papers by this author First published: 1995 https://doi.org/10.1002/humu.1380060314Citations: 5AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. 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Singh I, Moser AE, Moser HW, Kishimoto Y (1984) Adrenoleukodystrophy: Impaired Oxidation of very long chain fatty acids in white blood cells, cultuted skin fibroblasts, and amniocytes. Pediatr Res 18: 286– 290. Uchiyama A, Suzuki Y, Song XQ, Fukao T, Imamura A, Tomatsu S, Shimozawa N, Kondo N, Orii T (1994) Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy. Biochem Biophys Res Commun 198: 632– 636. Warren ST, Knight SJL, Peters JF, Stayton CL, Consalez GG, Zhang F (1990) Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage. Proc Natl Acad Sci USA 87: 3856– 3860. Citing Literature Volume6, Issue31995Pages 263-267 ReferencesRelatedInformation

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