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Autor:
Sophia Colamarino, Roberta Zaninetti, Elena I. Rugarli, M. Piccolella, Cristiano Rumio, Flavio Piva, Roberto Maggi, Anna Cariboni, Federica Pimpinelli
Publikováno v:
Human Molecular Genetics. 13:2781-2791
X-linked Kallmann's syndrome (KS) is a genetic disease characterized by anosmia and hypogonadism due to impairment in the development of olfactory axons and in the migration of gonadotropin-releasing hormone (GnRH)-producing neurons. Deletions or poi