A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis.
作者信息
Morice-Picard Fanny, Léauté-Labrèze Christine, Décor Aude, Boralevi Franck, Lacombe Didier, Taieb Alain, Fischer Judith
机构信息
National Reference Centre for Rare Skin Disorders, INSERM U876, CHU de Bordeaux, Bordeaux, France.
出版信息
Am J Med Genet A. 2010 Oct;152A(10):2664-5. doi: 10.1002/ajmg.a.33648.
PMID:20815031
Abstract
摘要
Zotero 插件