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Xie HN 1
Showing records 1 to 1 | Display all abstracts from Xie HN82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wu X; Xie HN; Wu T; Liu W; Chen LL; Li ZH; Wang DJ; Wang Y; Huang HB
Experimental and therapeutic medicine 2019; 18: 2255-2261