✦ LIBER ✦
An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect
✍ Scribed by Alexandre Janer; Hana Antonicka; Emilie Lalonde; Tamiko Nishimura; Florin Sasarman; Garry K. Brown; Ruth M. Brown; Jacek Majewski; Eric A. Shoubridge
- Book ID
- 119184382
- Publisher
- American Society of Human Genetics
- Year
- 2012
- Tongue
- English
- Weight
- 627 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0002-9297
No coin nor oath required. For personal study only.