Open AccessFrequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism
Author(s) -
Taneli Raivio,
Yisrael Sidis,
Lacey Plummer,
Huaibin Chen,
Jinghong Ma,
Abir Mukherjee,
Elka Jacobson-Dickman,
Richard Quinton,
Guy Van Vliet,
Hélène B. Lavoie,
Virginia Hughes,
Andrew Dwyer,
Frances J. Hayes,
Shuyun Xu,
Susan Sparks,
Ursula B. Kaiser,
Moosa Mohammadi,
Nelly Pitteloud
Publication year - 2009
Publication title -
endocrine reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.357
H-Index - 272
eISSN - 1945-7189
pISSN - 0163-769X
DOI - 10.1210/edrv.30.7.9981
Subject(s) - kallmann syndrome , fibroblast growth factor receptor 1 , hypogonadotropic hypogonadism , biology , mutation , endocrinology , mutant , genetics , medicine , receptor tyrosine kinase , phenotype , receptor , fibroblast growth factor , gene , disease , hormone , covid-19 , infectious disease (medical specialty)
The Harvard Center for Reproductive Endocrine Sciences and the Reproductive Endocrine Unit of the Department of Medicine (T.R., Y.S., L.P., A.M., E.J.-D., V.A.H., A.D., F.J.H., N.P.), Massachusetts General Hospital, and Harvard Center for Reproductive Endocrine Sciences and Brigham and Women’s Hospital (S.X., U.B.K.), Division of Endocrinology, Diabetes, and Hypertension, Boston, Massachusetts 02114; Department of Pharmacology (H.C., J.M., M.M.), New York University School of Medicine, New York, New York 10016; Institute of Human Genetics (R.Q.), University of Newcastle-upon-Tyne, Newcastle NE2 4HH, United Kingdom; Sainte Justin Hospital (G.V.V.), Montréal, Québec, Canada H3T 1C5; Centre Hospitalier de l’Université de Montréal and Procrea Cliniques (H.L.), Montréal, Québec, Canada H2W1T8; Department of Genetics and Metabolism (S.S.), Children’s National Medical Center, Washington, DC 20010; and Biomedicum Helsinki (T.R.), Institute of Biomedicine/Physiology, University of Helsinki, FIN-00014 Helsinki, Finland
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