(Q61647463)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15941866%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

title

An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain (English)

1 reference

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12 January 2020

1 reference

1 reference

2

1 reference

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12 January 2020

Alexandru Saveanu

4

1 reference

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12 January 2020

Thierry Brue

9

1 reference

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12 January 2020

author name string

Rachel Reynaud

1

1 reference

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12 January 2020

Sophie Vallette-Kasic

3

1 reference

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12 January 2020

Marie-Pierre Guillet

5

1 reference

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12 January 2020

Gilbert Simonin

6

1 reference

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12 January 2020

Alain Enjalbert

7

1 reference

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12 January 2020

Paul Valensi

8

1 reference

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12 January 2020

language of work or name

English

0 references

publication date

7 June 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15941866%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Clinical Endocrinology and Metabolism

12 January 2020

published in

1 reference

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12 January 2020

volume

90

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12 January 2020

issue

8

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12 January 2020

page(s)

4880-4887

1 reference

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12 January 2020

Identifiers

DOI

10.1210/JC.2005-0119

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15941866%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference