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

Overview of attention for article published in Frontiers in Genetics, August 2022

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Identification of the first congenital ichthyosis case caused by a homozygous deletion in the <em>ALOX12B</em> gene due to chromosome 17 mixed uniparental disomy | Lei Zhang | https://t.co/PoguqMQPzL

25 Aug 2022

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New Research: Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy: Uniparental disomy (UPD) is a rare genetic event caused by errors during… https://t.co/j

08 Aug 2022

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