Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency.


Autoria(s): Trarbach E.B.; Abreu A.P.; Silveira L.F.; Garmes H.M.; Baptista M.T.; Teles M.G.; Costa E.M.; Mohammadi M.; Pitteloud N.; Mendonca B.B.; Latronico A.C.
Data(s)

2010

Identificador

https://serval.unil.ch/?id=serval:BIB_F6AF3D95AEF2

isbn:1945-7197[electronic], 0021-972X[linking]

pmid:20463092

doi:10.1210/jc.2010-0176

isiid:000279589600055

Idioma(s)

en

Fonte

Journal of Clinical Endocrinology and Metabolism, vol. 95, no. 7, pp. 3491-3496

Palavras-Chave #Codon, Nonsense/genetics; Fibroblast Growth Factor 8/genetics; Follicle Stimulating Hormone/blood; Humans; Hypogonadism/genetics; Luteinizing Hormone/blood; Male; Radioimmunoassay; Severity of Illness Index
Tipo

info:eu-repo/semantics/article

article