- Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL22016 | 1. lékařská fakulta
- Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 42018 | 1. lékařská fakulta, 3. lékařská fakulta
- Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF62016 | 1. lékařská fakulta
- Prevalence of mutations in AGPAT2 among human lipodystrophies2003 | 2. lékařská fakulta
- Mutations in HIV-1 gag and pol compensate for the loss of viral fitness caused by a highly mutated protease2012 | Přírodovědecká fakulta
- Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis2010 | 2. lékařská fakulta
- Po stopách genetických příčin chronického onemocnění ledvin2021 | 1. lékařská fakulta
