A comparative phenotypic study of Kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 (PROK2) or prokineticin receptor 2 (PROKR2) genes
Year: 2011
Type: dissertation
Authors: SARFATI, Julie, YOUNG, Jacques
Language: English
Subfield: Reproductive Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W7018062972
