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Bashir R 1

Showing records 1 to 1 | Display all abstracts from Bashir R

107890 Exome Sequencing Reveals Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
Yousaf K; Naz S; Mushtaq A; Wohler E; Sobreira N; Ho BM; Chen LJ; Chu WK; Bashir R
Genes 2023; 14:

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