Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q

Myodystrophy (myd) is an autosomal‐recessive mouse mutation with dystrophic skeletal muscle. We propose that myd may be a model of the human disorder facioscapulohumeral dystrophy (FSHD) on the basis of clinical features and homologous genetic map locations. FSHD maps to human 4q35, while myd maps t...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Muscle & nerve 1995, Vol.18 (S13), p.S98-S102
Hauptverfasser:	Mathews, Katherine D., Mills, Kathleen A., Bailey, Holly L., Schelper, Robert L., Murray, Jeffrey C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Diseases of striated muscles. Neuromuscular diseases facioscapulohumeral dystrophy human chromosome 4 kallikrein Medical sciences mouse chromosome 8 myodystrophy mutation Neurology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!