(PDF) Comparing Histopathology From Patients With X-Linked

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

Journal of the American Academy of Dermatology - United States

doi 10.1016/j.jaad.2015.12.027

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Date

May 1, 2016

Authors

Leslie Robinson-Bostom

Publisher

Elsevier BV

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Amanote Research

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

Journal of the American Academy of Dermatology - United States

doi 10.1016/j.jaad.2015.12.027

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient

Novel Transglutaminase-1 Mutations and Genotype-Phenotype Investigations of 104 Patients With Autosomal Recessive Congenital Ichthyosis in the USA

Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis

Transglutaminase 1 Mutations in Autosomal Recessive Congenital Ichthyosis: Private and Recurrent Mutations in an Isolated Population

Autosomal Recessive Congenital Ichthyosis: CERS3 Mutations Identified by a Next Generation Sequencing Panel Targeting Ichthyosis Genes

375 Modelling and Understanding Pathomechanisms of X-Linked Recessive Ichthyosis in Vitro

Increased Prevalence of Filaggrin Deficiency in 51 Patients With Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

NIPAL4 Deletion Identified in an American Bully With Autosomal Recessive Congenital Ichthyosis and Response to Topical Therapy

Targeted Regions Sequencing Identified Four Novel PNPLA1 Mutations in Two Chinese Families With Autosomal Recessive Congenital Ichthyosis