Polubothu, S;
A-Olabi, L;
Carmen Del Boente, M;
Chacko, A;
Eleftheriou, G;
Glover, M;
Jiménez-Gallo, D;
... Kinsler, VA; + view all
(2020)
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
, 140
(5)
pp. 1110-1113.
10.1016/j.jid.2019.10.019.
Preview |
Text
1-s2.0-S0022202X19334785-main.pdf - Accepted Version Download (17MB) | Preview |
| Type: | Article |
|---|---|
| Title: | GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of Gα/11 Mosaicism and the Associated Clinical Diagnoses |
| Location: | United States |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1016/j.jid.2019.10.019 |
| Publisher version: | https://doi.org/10.1016/j.jid.2019.10.019 |
| Language: | English |
| Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions. |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Genetics and Genomic Medicine Dept |
| URI: | https://discovery.ucl.ac.uk/id/eprint/10088470 |
Archive Staff Only
 |
View Item |
