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Triallelic Inheritance of TGM1 and ALOXE3 Mutations Associated with Severe Phenotype of Ichtyosis in an Iranian Family - A Case Report

Lamellar ichthyosis is one form of congenital autosomal recessive ichthyosis. To date, seven causative genes for ARCI have been identified. To understand further the genetic spectrum of the disease, we analyzed a four-generation Iranian family with ARCI that had observable inheritance. Exome sequenc...

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Detalhes bibliográficos
Publicado no:Iran J Public Health
Main Authors: AKBARI, Mohammad Taghi, ATAEI-KACHOUI, Mojgan
Formato: Artigo
Idioma:Inglês
Publicado em: Tehran University of Medical Sciences 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4645748/
https://ncbi.nlm.nih.gov/pubmed/26576379
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