Olmsted syndrome in an Indian male with a newde novomutation inTRPV3

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

(2014) S. Duchatelet et al.   BRITISH JOURNAL OF DERMATOLOGY

Olmsted syndrome in an Iranian boy with a newde novomutation inTRPV3

(2014) A. Kariminejad et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY

Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3

(2014) Ori Eytan et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

A NewTRPV3Missense Mutation in a Patient With Olmsted Syndrome and Erythromelalgia

(2014) Sabine Duchatelet et al.   JAMA Dermatology

Recurrent splice-site mutation in MBTPS2underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patient

(2013) H. J. Wang et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY

Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted Syndrome

(2012) Zhimiao Lin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome

(2012) J.E. Lai-Cheong et al.   BRITISH JOURNAL OF DERMATOLOGY

A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted Syndrome

(2012) Alireza Haghighi et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY