✦ LIBER ✦
Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing
✍ Scribed by Eri Kondo; Takafumi Nishimura; Tomoki Kosho; Yuji Inaba; Satomi Mitsuhashi; Takefumi Ishida; Atsushi Baba; Kenichi Koike; Ichizo Nishino; Ikuya Nonaka; Toru Furukawa; Kayoko Saito
- Book ID
- 111995089
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 496 KB
- Volume
- 158A
- Category
- Article
- ISSN
- 1552-4825
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