(Q47691112)

English

PIK3R1 mutations in SHORT syndrome.

scientific article published on 17 October 2013

In more languages

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scholarly article

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

PIK3R1 mutations in SHORT syndrome. (English)

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

author name string

C Schroeder

1

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

A Riess

2

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

M Bonin

3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

P Bauer

4

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

O Riess

5

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

M Döbler-Neumann

6

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

S Wieser

7

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

U Moog

8

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

A Tzschach

9

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

publication date

17 October 2013

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

Clinical Genetics

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

86

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

292-294

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12263

21 January 2018

Mutations in PIK3R1 cause SHORT syndrome

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12263

21 January 2018

SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12263

21 January 2018

PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12263

21 January 2018

SHORT syndrome and insulin resistance

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12263

21 January 2018

Identifiers

10.1111/CGE.12263

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/23980586

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