advertisement

---

Duran D 1

Showing records 1 to 1 | Display all abstracts from Duran D

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

---