Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1.

We recently described an autosomal dominant inclusion-body myopathy characterized by congenital joint contractures, external ophthalmoplegia, and predominantly proximal muscle weakness. A whole-genome scan, performed with 161 polymorphic markers and with DNA from 40 members of one family, indicated...

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Bibliographische Detailangaben
Hauptverfasser: Martinsson, T, Darin, N, Kyllerman, M, Oldfors, A, Hallberg, B, Wahlström, J
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1999
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377880/
https://ncbi.nlm.nih.gov/pubmed/10205275
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