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

JOURNAL OF INVESTIGATIVE DERMATOLOGY (2020)

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Journal

JOURNAL OF INVESTIGATIVE DERMATOLOGY
Volume 140, Issue 5, Pages 1110-1113

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jid.2019.10.019

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Categories

Dermatology

Funding

  1. Wellcome Trust [WT104076MA]
  2. Caring Matters Now Charity
  3. Newlife Foundation
  4. GOSHCC Livingstone Skin Research Centre
  5. UK National Institute for Health Research through the Biomedical Research Centre at Great Ormond St Hospital for Children NHS Foundation Trust
  6. UCL GOS Institute of Child Health

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