Xu Cao
Beijing, China
Last Updated: 09/26/2026
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Found 8 publications
Genotype‒Phenotype Correlation of TRPV3-Related Olmsted Syndrome.
Journal: The Journal of investigative dermatology
Published: November 04, 2019
Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia.
Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric Erythrokeratodermia.
Journal: The Journal of investigative dermatology
Published: June 12, 2018
Semidominant Inheritance in Olmsted Syndrome.
Journal: The Journal of investigative dermatology
Published: January 11, 2016
Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis.
Journal: Gene
Published: December 18, 2014
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome.
Journal: Human molecular genetics
Published: August 30, 2014
New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosis.
Journal: The Journal of investigative dermatology
Published: February 12, 2014
Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type.
Journal: The Journal of investigative dermatology
Published: July 23, 2013
Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome.
Journal: American journal of human genetics
Published: November 25, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026