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1-2 of 2 results for P2RX2

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Select article: Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

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Research article

First published May, 2015

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Hideaki Moteki, Hela Azaiez, Kevin T. Booth [...]

Annals of Otology,Rhinology & Laryngology

Select article: Efficient introduction of an isogenic homozygous mutation to induced pluripotent stem cells from a hereditary hearing loss family using CRISPR/Cas9 and single-stranded donor oligonucleotides

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Research article

First published April, 2019

Efficient introduction of an isogenic homozygous mutation to induced pluripotent stem cells from a hereditary hearing loss family using CRISPR/Cas9 and single-stranded donor oligonucleotides

Yunpeng Dong, Tao Peng, Weijing Wu [...]

Journal of International Medical Research

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