Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54 (Q24685744)

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Emmanuelle Génin

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Jean-Claude Carel

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Fumihiko Matsuda

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Jean-Louis Chaussain

Proceedings of the National Academy of Sciences of the United States of America

5

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language of work or name

English

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publication date

16 September 2003

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published in

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volume

100

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page(s)

10972-6

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issue

19

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cites work

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The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54

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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

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Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions

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Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism

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12 December 2020

Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions

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12 December 2020

Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19

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12 December 2020

Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations

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12 December 2020

Identifiers

DOI

10.1073/PNAS.1834399100

1 reference

308270

ADS bibcode

2003PNAS..10010972D

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308270

1 reference

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