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A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs
- 1.Huranová, M., Hnilicová, J., Fleischer, B., Cvačková, Z., Staněk, D. A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs. Human Molecular Genetics. 2009, 18(11), 2014-2023. ISSN 0964-6906. E-ISSN 1460-2083. Dostupné z: doi: 10.1093/hgm/ddp125
Počet záznamů: 1