Molecular assessment of autosomal dominant hypotrichosis
收藏NIAID Data Ecosystem2026-03-11 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA625422
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资源简介：
This study involves the genetic characterisation of five patients with congenital hypotrichosis from a multigenerational pedigree where the disease segregates in autosomal dominant fashion. The aim is to provide a diagnosis and better clinical management, as well as provide broader insights into the mechanisms of hypotrichosis.
创建时间：
2020-04-15
