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  1. Article

    Open Access

    TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia

    Skeletal dysplasia is a common, clinically and genetically heterogeneous disorder in the human population. An increasing number of different genes are being identified causing this disorder. We used whole exom...

    Mahsa Sadat Asl Mohajeri, Atieh Eslahi, Zeinab Khazaii… in Human Genomics (2021)

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