![](/img/cover-not-exists.png)
The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes
Raquel M. Fernández, Guillermo Antiñolo, Charis Eng, Salud BorregoVolume:
22
Year:
2003
Language:
english
Pages:
4
DOI:
10.1002/humu.10273
File:
PDF, 105 KB
english, 2003