Publication | Closed Access
A new mutation (Leu569Arg) within Exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I
82
Citations
21
References
2003
Year
New MutationMendelian DisorderOphthalmologyCorneal DystrophyGenetic DisorderGeneticsExon 13Molecular GeneticsDisease Gene IdentificationMedicine
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