A Plakophilin-1 Gene Mutation in an Egyptian Family With Ectodermal Dysplasia-Skin Fragility Syndrome

Molecular Syndromology - Switzerland
doi 10.1159/000369267
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

S. Karger AG

Related search

Cerebellar Ataxia-Ectodermal Dysplasia Syndrome

2020English

Ectodermal Dysplasia-Sensorineural Deafness Syndrome

2020English

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American Journal of Human Genetics
Genetics
2014English

Mutation Identification in a Canine Model of X-Linked Ectodermal Dysplasia

Mammalian Genome
Genetics
2005English

Contractures-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome

2020English

Hypohidrotic Ectodermal Dysplasia

2020English

231 a Mutation in the SAM Domain of P63 Causing a Mild Ectodermal Dysplasia Phenotype

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2017English

Hypohidrotic Ectodermal Dysplasia in Association With Athelia

Journal of Genetic Syndromes & Gene Therapy
2014English

Odontomicronychial Ectodermal Dysplasia.

Journal of Medical Genetics
Genetics
1996English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy