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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Crossref DOI link: https://doi.org/10.1038/s41436-020-01087-5

Published Print: 2021-06

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Kotan, Leman Damla

Ternier, Gaetan

Cakir, Aydilek Dagdeviren

Emeksiz, Hamdi Cihan

Turan, Ihsan

Delpouve, Gaspard

De Kardelen, Asli rya

Ozcabi, Bahar

Isik, Emregul

Mengen, Eda

De Cakir, Esra niz P.

Yuksel, Aysegul

Agladioglu, Sebahat Yilmaz

Dilek, Semine Ozdemir

Evliyaoglu, Olcay

Darendeliler, Feyza

Gurbuz, Fatih

Akkus, Gamze

Yuksel, Bilgin

Giacobini, Paolo

Topaloglu, A. Kemal https://orcid.org/0000-0003-2931-9552
Funding

Funding for this research was provided by:

INSERM (U1172, U1172)

European Research Council (725149/REPRODAMH)
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Version of Record valid from 2022-06-01
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This article is maintained by: Elsevier

Article Title: Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-01087-5

Content Type: article

Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics

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