
Point mutation in a Becker muscular dystrophy patient
1993; Oxford University Press; Volume: 2; Issue: 1 Linguagem: Inglês
10.1093/hmg/2.1.75
ISSN1460-2083
AutoresRoland G. Roberts, Maria Rita Passos‐Bueno, Martin Bobrow, Mariz Vainzof, Mayana Zatz,
Tópico(s)Muscle Physiology and Disorders
ResumoJournal Article Point mutation in a Becker muscular dystrophy patient Get access Roland G. Roberts, Roland G. Roberts * * To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Maria Rita Passos-Bueno, Maria Rita Passos-Bueno 1Departmento de Biologia, Instituto de Biociências, Universidade de Sāo PauloSP, Brazil Search for other works by this author on: Oxford Academic PubMed Google Scholar Martin Bobrow, Martin Bobrow Search for other works by this author on: Oxford Academic PubMed Google Scholar Mariz Vainzof, Mariz Vainzof 1Departmento de Biologia, Instituto de Biociências, Universidade de Sāo PauloSP, Brazil Search for other works by this author on: Oxford Academic PubMed Google Scholar Mayana Zatz Mayana Zatz 1Departmento de Biologia, Instituto de Biociências, Universidade de Sāo PauloSP, Brazil Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 2, Issue 1, January 1993, Pages 75–77, https://doi.org/10.1093/hmg/2.1.75 Published: 01 January 1993 Article history Received: 08 October 1992 Revision received: 20 November 1992 Accepted: 20 November 1992 Published: 01 January 1993
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