Showing 1 - 2 results of 2 for search '"MARVELD2"', query time: 0.06s Refine Results
  1. 1
    Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families

    Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families by Xinyu Shi, Xiaozhou Liu, Yanjun Zong, Zhengdong Zhao, Yu Sun

    Published 2024-08-01
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  2. 2
    Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family

    Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family by Chuican Huang, Zhenning Huang, Ping Wang, Xijing Wu, Xijing Wu, Qiaomiao Zhou, Jun Ding, Qing Luo, Weijia Wu, Xialin Fan, Lichun Fan, Lichun Fan

    Published 2024-12-01
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