✦ LIBER ✦
A Novel De Novo Mutation of theTITF1/NKX2-1Gene Causing Ataxia, Benign Hereditary Chorea, Hypothyroidism and a Pituitary Mass in a UK Family and Review of the Literature
✍ Scribed by Veneziano, Liana; Parkinson, Michael H.; Mantuano, Elide; Frontali, Marina; Bhatia, Kailash P.; Giunti, Paola
- Book ID
- 125380465
- Publisher
- Springer-Verlag
- Year
- 2014
- Tongue
- English
- Weight
- 549 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1473-4222
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