Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome.

CONCLUSION: A novel mutation in the KCNQ1 gene is described. There may be less frequency of mutations in the KCNQ1 and of KCNE1 genes in Iranian JLNS patients compared with other populations. PMID: 30942114 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/30942114?dopt=Abstract

Source: Fetal and Pediatric Pathology - April 4, 2019 Category: Pathology Tags: Fetal Pediatr Pathol Source Type: research