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Whole-exome Sequencing Identified a Novel Hemizygous Missense Variant in the EDA Gene in an Iranian Patient Causing Hypohidrotic Ectodermal Dysplasia
Whole-exome Sequencing Identified a Novel Hemizygous Missense Variant in the EDA Gene in an Iranian Patient Causing Hypohidrotic Ectodermal Dysplasia

Saeed Dorgaleleh; Morteza Oladnabi

Volume 10, Issue 9 , September 2022, , Pages 16641-16649

https://doi.org/10.22038/ijp.2022.66620.4998

Abstract
  Ectodermal dysplasia (ED) is a congenital heterogenic disorder caused by the defect in the ectoderm and its derivatives. This complex disorder has different subtypes, the most common ...  Read More