GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses-Reference-Cited by-同舟云学术

GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses

Published:2020-05 Issue:5 Volume:140 Page:1110-1113
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Polubothu Satyamaanasa^ORCID,Al-Olabi Lara^ORCID,Carmen del Boente Maria^ORCID,Chacko Alisha^ORCID,Eleftheriou Georgios^ORCID,Glover Mary^ORCID,Jiménez-Gallo David^ORCID,Jones Elizabeth A.^ORCID,Lomas Debra^ORCID,Fölster-Holst Regina^ORCID,Syed Samira^ORCID,Tasani Monika^ORCID,Thomas Anna^ORCID,Tisdall Martin^ORCID,Torrelo Antonio^ORCID,Aylett Sarah^ORCID,Kinsler Veronica A.^ORCID

Funder

Wellcome Trust

Caring Matters Now Charity

Newlife Foundation

GOSHCC Livingstone Skin Research Centre

UK National Institute for Health Research

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference14 articles.

1. Somatic activating mutations in GNAQ and GNA11 are associated with congenital hemangioma;Ayturk;Am J Hum Genet,2016