z-logo
open-access-imgOpen Access
GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants inKISS1/Kiss1
Author(s) -
Yee-Ming Chan,
Sarabeth BroderFingert,
Sophia Paraschos,
Risto Lapatto,
Margaret Au,
Virginia Hughes,
Suzy D.C. Bianco,
Le Min,
Lacey Plummer,
Felecia Cerrato,
Adelaide de Guillebon,
I-Hsuan Wu,
Fazal Wahab,
Andrew Dwyer,
Susan Kirsch,
Richard Quinton,
Timothy Cheetham,
Metin Özata,
Svetlana Ten,
JeanPierre Chanoine,
Nelly Pitteloud,
Kathryn A. Martin,
Raphael Schiffmann,
H.J. van der Kamp,
Shahla Nader,
Janet E. Hall,
Ursula B. Kaiser,
Stephanie B. Seminara
Publication year - 2011
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2011-0518
Subject(s) - endocrinology , medicine , kisspeptin , biology , heterozygote advantage , proband , allele , genetics , gene , mutation , hypothalamus
KISS1 is a candidate gene for GnRH deficiency.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom