✦ LIBER ✦
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation
✍ Scribed by Hideo Sugie; Yoko Sugie; Masataka Ito; Tokiko Fukuda; Ikuya Nonaka; Yoshio Igarashi
- Book ID
- 115828194
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 361 KB
- Volume
- 236
- Category
- Article
- ISSN
- 0009-8981
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