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Nelson-Williams C 1

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70834 Digenic mutations of human OCRL paralogs in Dent's disease type 2 associated with Chiari I malformation
Duran D; Jin SC; DeSpenza T; Nelson-Williams C; Cogal AG; Abrash EW; Harris PC; Lieske JC; Shimshak SJ; Mane S; Bilguvar K; DiLuna ML; Günel M; Lifton RP; Kahle KT
Human genome variation 2016; 3: 16042

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