✦ LIBER ✦
Two novel RRM2B gene mutations in a patient with autosomal recessive progressive external ophthalmoplegia, encephalopathy and cytochrome c oxidase deficiency
✍ Scribed by Natalie S. Hauser; Renkui Bai
- Book ID
- 119327003
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 75 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1567-7249
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