TheRETC620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes (Q57591210)
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scientific article published on 01 November 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | TheRETC620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes |
scientific article published on 01 November 2003 |
Statements
The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes (English)
Guillermo Antiñolo
Salud Borrego
Raquel M Fernández
1 November 2003
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