✦ LIBER ✦
The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes
✍ Scribed by Raquel M. Fernández; Guillermo Antiñolo; Charis Eng; Salud Borrego
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 105 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1059-7794
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