Yüklüyor......

Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is a neuromuscular disorder characterized by an insidious onset and progressive course. The disease has a frequency of about 1 in 20,000 and is transmitted in an autosomal dominant fashion with almost complete penetrance. Deletion of an integral number o...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Tupler, Rossella, Perini, Giovanni, Pellegrino, Maria Antonietta, Green, Michael R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The National Academy of Sciences 1999
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC23032/
https://ncbi.nlm.nih.gov/pubmed/10535977
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!