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Allan–Herndon–Dudley syndrome (AHDS) in two consecutive generations caused by a missense MCT8 gene mutation. Phenotypic variability with the presence of normal serum T3 levels
✍ Scribed by Boccone, Loredana; Dessì, Valentina; Meloni, Antonella; Loudianos, Georgios
- Book ID
- 125441195
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 450 KB
- Volume
- 56
- Category
- Article
- ISSN
- 1769-7212
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