- Tytuł:
- Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1.
- Autorzy:
- Temat:
-
FACIOSCAPULOHUMERAL muscular dystrophy
MUSCLE abnormalities
METHYLATION kinetics
SHOULDER girdle
CHROMOSOME abnormalities
DISEASES - Źródło:
- European Journal of Human Genetics. Jun2015, Vol. 23 Issue 6, p808-816. 9p.
Czasopismo naukowe