Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient
Mayumi Abe, Itsuro Higuchi, Hiroko Morisaki, Takayuki Morisaki, Mitsuhiro OsameVolume:
10
Year:
2000
Language:
english
DOI:
10.1016/s0960-8966(00)00127-9
File:
PDF, 1.67 MB
english, 2000