Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
| Autor: | Dode, Catherine, Levilliers, Jacqueline, Dupont, Jean-Michel, De Paepe, Anne, Le Du, Nathalie, Soussi-Yanicostas, Nadia, Coimbra, Roney S., Delmaghani, Sedigheh, Compain-Nouaille, Sylvie, Baverel, Francoise, Pecheux, Christophe, Le Tessier, Dominique, Cruaud, Corinne, Delpech, Marc, Speleman, Frank, Vermeulen, Stefan, Amalfitano, Andrea, Bachelot, Yvan, Bouchard, Philippe |
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| Zdroj: | Nature Genetics. Apr2003, Vol. 33 Issue 4, p463. 3p. |
| Databáze: | Academic Search Ultimate |
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