Diagnóstico oftalmológico del síndrome de linfedema-distiquiasis a través de la mutación FOXC2-Reference-Cited by-同舟云学术

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Diagnóstico oftalmológico del síndrome de linfedema-distiquiasis a través de la mutación FOXC2

Published:2024-04 Issue:4 Volume:99 Page:177-180
ISSN:0365-6691
Container-title:Archivos de la Sociedad Española de Oftalmología
language:es
Short-container-title:Archivos de la Sociedad Española de Oftalmología

Author:

Calleja Casado F.,Ortega Prades G.,Lanuza García A.,Duch Samper A.

Publisher

Elsevier BV

Reference8 articles.

1. Distichiasis: An update on etiology, treatment and outcomes;Singh;Indian J Ophthalmol.,2022

2. FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function;Tavian;Oncotarget.,2016

3. Novel FOXC2 mutation in hereditary distichiasis impairs DNA-binding activity and transcriptional activation;Zhang;Int J Biol Sci.,2016

4. Lymphedema-distichiasis syndrome;Mansour;GeneReviews®,1993

5. Lymphedema-distichiasis syndrome: A distinct type of primary lymphedema caused by mutations in the FOXC2 gene;Vreeburg;Int J Dermatol.,2008

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