Lhfpl4-flox 基因敲除小鼠

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3. Kalay, Ersan, Li, Yun, Uzumcu, Abdullah, Kremer, Hannie, Wollnik, Bernd. . Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. In Human mutation, 27, 633-9. doi:. https://pubmed.ncbi.nlm.nih.gov/16752389/

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