Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

Zhang, Lei; Hu, Yanqiu; Lu, Jingjing; Zhao, Peiwei; Zhang, Xiankai; Tan, Li; Li, Jun; Xiao, Cuiping; Zeng, Linkong; He, Xuelian

doi:10.3389/fgene.2022.931833

Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

Lei Zhang, et al.

ByLei Zhang

Aug 8, 2022 alh5, ALOX12B, brh5Lei, Case, caused, chromosome, congenital, deletion, disomy, due, Gene, homozygous, ichthyosis, Identification, Mixed, Uniparental, Zhang

Frontiers | Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

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Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

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