A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene
1992; Oxford University Press; Volume: 1; Issue: 2 Linguagem: Inglês
10.1093/hmg/1.2.123
ISSN1460-2083
AutoresJeremy P. Cheadle, Alison L. Meredith, Layla N. Al-Jader,
Tópico(s)Neurogenetic and Muscular Disorders Research
ResumoJournal Article A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene Get access Jeremy P. Cheadle, Jeremy P. Cheadle Institute of Medical Genetics, University of Wales College of MedicineCardiff CF4 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Alison L. Meredith, Alison L. Meredith Institute of Medical Genetics, University of Wales College of MedicineCardiff CF4 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Layla N. Al-Jader Layla N. Al-Jader Institute of Medical Genetics, University of Wales College of MedicineCardiff CF4 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 1, Issue 2, May 1992, Pages 123–125, https://doi.org/10.1093/hmg/1.2.123 Published: 01 May 1992 Article history Received: 23 January 1992 Published: 01 May 1992
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