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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

✍ Scribed by Dodé, Catherine; Levilliers, Jacqueline; Dupont, Jean-Michel; De Paepe, Anne; Le Dû, Nathalie; Soussi-Yanicostas, Nadia; Coimbra, Roney S.; Delmaghani, Sedigheh; Compain-Nouaille, Sylvie; Baverel, Françoise

Book ID: 109918473
Publisher: Nature Publishing Group
Year: 2003
Tongue: English
Weight: 85 KB
Volume: 33
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1122

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