Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation (Q52208872)
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scientific article published on April 30, 1995
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation |
scientific article published on April 30, 1995 |
Statements
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation (English)
H. Sugie
Y. Sugie
M. Ito
T. Fukuda
I. Nonaka
1 April 1995
1 reference
236
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1
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81-86
1 reference