✦ LIBER ✦
LAMA2 stop-codon mutation: Merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression
✍ Scribed by Piernanda Vigliano; Patrizia Dassi; Claudia Di Blasi; Marina Mora; Laura Jarre
- Book ID
- 113590322
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 939 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1090-3798
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