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serval:BIB_C988869DDA2B
A genetic basis for functional hypothalamic amenorrhea.
10.1056/NEJMoa0911064
000286383900006
21247312
Caronia
L.M.
author
Martin
C.
author
Welt
C.K.
author
Sykiotis
G.P.
author
Quinton
R.
author
Thambundit
A.
author
Avbelj
M.
author
Dhruvakumar
S.
author
Plummer
L.
author
Hughes
V.A.
author
Seminara
S.B.
author
Boepple
P.A.
author
Sidis
Y.
author
Crowley
W.F.
author
Martin
K.A.
author
Hall
J.E.
author
Pitteloud
N.
author
article
2011
New England Journal of Medicine
1533-4406[electronic], 0028-4793[linking]
journal
364
3
215-225
Amenorrhea/etiology
Amenorrhea/genetics
Extracellular Matrix Proteins/genetics
Female
Gene Expression
Genetic Predisposition to Disease
Gonadotropin-Releasing Hormone/deficiency
Gonadotropin-Releasing Hormone/genetics
Humans
Hypogonadism/genetics
Hypothalamic Diseases/complications
Hypothalamic Diseases/genetics
Luteinizing Hormone/secretion
Mutation
Nerve Tissue Proteins/genetics
Protein Precursors/genetics
Receptor, Fibroblast Growth Factor, Type 1/genetics
Receptors, G-Protein-Coupled/genetics
Receptors, LHRH/genetics
Receptors, Peptide/genetics
Sequence Analysis, DNA
eng
60_published
true
peer-reviewed
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https://serval.unil.ch/resource/serval:BIB_C988869DDA2B.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C988869DDA2B4
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