advertisement
Vishwakarma S 1
Showing records 1 to 1 | Display all abstracts from Vishwakarma S91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Senthil S; Sharma S; Vishwakarma S; Kaur I
Ophthalmic Genetics 2021; 42: 28-34
