GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.


Autoria(s): Chan Y.M.; Broder-Fingert S.; Paraschos S.; Lapatto R.; Au M.; Hughes V.; Bianco S.D.; Min L.; Plummer L.; Cerrato F.; De Guillebon A.; Wu I.H.; Wahab F.; Dwyer A.; Kirsch S.; Quinton R.; Cheetham T.; Ozata M.; Ten S.; Chanoine J.P.; Pitteloud N.; Martin K.A.; Schiffmann R.; Van der Kamp H.J.; Nader S.; Hall J.E.; Kaiser U.B.; Seminara S.B.
Data(s)

2011

Identificador

http://serval.unil.ch/?id=serval:BIB_F112A82B2C69

isbn:1945-7197 (Electronic)

pmid:21880801

doi:10.1210/jc.2011-0518

isiid:000296750600007

Idioma(s)

en

Fonte

Journal of Clinical Endocrinology and Metabolism, vol. 96, no. 11, pp. E1771-E1781

Palavras-Chave #Adult; Animals; Female; Genotype; Gonadotropin-Releasing Hormone/deficiency; Heterozygote; Humans; Kisspeptins/genetics; Male; Mice; Phenotype
Tipo

info:eu-repo/semantics/article

article