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Publications by E Sbidian
Novel Mutation in GJB4 Gene (Connexin 30.3) in a Family With Erythrokeratodermia Variabilis
Acta Dermato-Venereologica
Dermatology
Medicine
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A Sporadic Case of Erythrokeratodermia Variabilis in an Adult
463 GJA1 Mutations Causing Erythrokeratodermia Variabilis Et Progressiva Display Increased Connexin Hemichannel Activity
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Mutation in the Connexin 50 Gene (GJA8) in a Russian Family With Zonular Pulverulent Cataract
Clinical Genetics
Genetics
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
Case of Erythrokeratodermia Variabilis Successfully Treated With Narrowband Ultraviolet B
Journal of Dermatology
Dermatology
Medicine
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Frontiers in Genetics
Genetics
Molecular Medicine
Pre-Implantation Genetic Diagnosis in an Iranian Family With a Novel Mutation in MUT Gene
BMC Medical Genetics
Genetics
A Novel Missense Mutation in the CYLD Gene in a Spanish Family With Multiple Familial Trichoepithelioma
Archives of Dermatology
Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
Journal of Zhejiang University: Science B
Genetics
Pharmacology
Molecular Biology
Biochemistry
Veterinary
Medicine
Toxicology
Pharmaceutics