Chromosome 4q;10q translocations; Comparison with different ethnic populations and FSHD patients

BACKGROUND: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder characterized by the weakness of facial, shoulder-girdle and upper arm muscles. Most patients with FSHD have fewer numbers of tandem repeated 3.3-kb KpnI units on chromosome 4q35. Chromosome 10q26 contains hi...

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Detalles Bibliográficos
Autores principales: Matsumura, Tsuyoshi, Goto, Kanako, Yamanaka, Gaku, Lee, Je Hyeon, Zhang, Cheng, Hayashi, Yukiko K, Arahata, Kiichi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC122075/
https://www.ncbi.nlm.nih.gov/pubmed/12188928
http://dx.doi.org/10.1186/1471-2377-2-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC122075/
https://www.ncbi.nlm.nih.gov/pubmed/12188928
http://dx.doi.org/10.1186/1471-2377-2-7

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