Pages that link to "Q81059628"
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The following pages link to TGFBI gene mutation analysis in families with hereditary corneal dystrophies from Ukraine (Q81059628):
Displaying 7 items.
- Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3) (Q34081492) (← links)
- TGFBI gene mutations in a Korean population with corneal dystrophy (Q34372236) (← links)
- TGFBI gene mutations in corneal dystrophies. (Q36472661) (← links)
- Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene (Q36639811) (← links)
- Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6. (Q37371325) (← links)
- TGFBI gene mutations in Brazilian patients with corneal dystrophy. (Q54620548) (← links)
- Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis (Q59388282) (← links)