✦ LIBER ✦
Clinical exome sequencing leads to the diagnosis of mitochondrial complex I deficiency in a family with global developmental delays, ataxia, and cerebellar and pons hypoplasia
✍ Scribed by Kimonis, Virginia; Gonzalez, Kelly; Zeng, Wenqi; Gray, Phillip; Tang, Sha; Wei, Jennifer; Li, X.; Lu, HM.; Lu, H.; Chao, Elizabeth
- Book ID
- 122131855
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 48 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1567-7249
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