Search Results - Kim, Jeonhyun

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    Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies

    Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies by Jin, Hyun-Seok, Kim, Jeonhyun, Kwak, Woori, Jeong, Hyeonsoo, Lim, Gyu-Bin, Lee, Cha Gon

    Published in PloS one
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