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DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
10.1093/hmg/ddx408
000424494900012
29202173
Bouilly
J.
author
Messina
A.
author
Papadakis
G.
author
Cassatella
D.
author
Xu
C.
author
Acierno
J.S.
author
Tata
B.
author
Sykiotis
G.
author
Santini
S.
author
Sidis
Y.
author
Elowe-Gruau
E.
author
Phan-Hug
F.
author
Hauschild
M.
author
Bouloux
P.M.
author
Quinton
R.
author
Lang-Muritano
M.
author
Favre
L.
author
Marino
L.
author
Giacobini
P.
author
Dwyer
A.A.
author
Niederländer
N.J.
author
Pitteloud
N.
author
article
2018-01-15
Human molecular genetics
1460-2083
0964-6906
journal
27
2
359-372
Adult
Cohort Studies
DCC Receptor/genetics
DCC Receptor/metabolism
Female
Fibronectin Type III Domain
Gonadotropin-Releasing Hormone/deficiency
Humans
Hypogonadism/genetics
Hypogonadism/metabolism
Hypogonadism/pathology
Male
Mutation
Netrin-1/genetics
Netrin-1/metabolism
Neurons/metabolism
Neurons/pathology
Pedigree
Whole Exome Sequencing
eng
60_published
true
peer-reviewed
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
https://serval.unil.ch/notice/serval:BIB_E34B12561F91
https://serval.unil.ch/resource/serval:BIB_E34B12561F91.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_E34B12561F914
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