FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies (Q35458207)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25759380%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

title

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies (English)

1 reference

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Ana Claudia Latronico Xavier

2 March 2020

author

4

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2 March 2020

Luciani Renata Carvalho

6

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2 March 2020

Mirian Yumie Nishi

12

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Berenice Bilharinho Mendonca

2 March 2020

17

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2 March 2020

16

Nelly Pitteloud

1 reference

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2 March 2020

author name string

Fernanda A Correa

1

1 reference

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2 March 2020

Ericka B Trarbach

2

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2 March 2020

Cintia Tusset

3

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2 March 2020

Luciana R Montenegro

5

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2 March 2020

Marcela M Franca

7

1 reference

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2 March 2020

Aline P Otto

8

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2 March 2020

Everlayny F Costalonga

9

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2 March 2020

Vinicius N Brito

10

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2 March 2020

Ana Paula Abreu

11

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2 March 2020

Alexander A L Jorge

13

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2 March 2020

Ivo J P Arnhold

14

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2 March 2020

Yisrael Sidis

15

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2 March 2020

publication date

10 March 2015

1 reference

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2 March 2020

published in

Endocrine Connections

1 reference

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2 March 2020

volume

4

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2 March 2020

page(s)

100-107

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2 March 2020

issue

2

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Creative Commons Attribution-NonCommercial 4.0 International

2 March 2020

copyright license

start time

1 June 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4401104/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.

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Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia

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Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

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PubMed

https://pubmed.ncbi.nlm.nih.gov/25759380

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1530/EC-15-0015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25759380%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25759380%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference