Publication | Closed Access
Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I
76
Citations
14
References
2005
Year
Novel MutationChinese FamilyMendelian DisorderOphthalmologyCorneal DystrophyGenetic DisorderGeneticsTgfbi GeneMolecular GeneticsDisease Gene IdentificationMedicine
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