✦ LIBER ✦
Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: Identification of 10 new mutations. Absence of genotype–phenotype correlation
✍ Scribed by Robert Aquaron; Jean-louis Bergé-Lefranc; Jean-Francois Pellissier; Marie-France Montfort; Michèle Mayan; Dominique Figarella-Branger; Michelle Coquet; Georges Serratrice; Jean Pouget
- Book ID
- 116792794
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 103 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0960-8966
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