Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family
Acta ophthalmologica.
2011 Mar ;
89 (2) :
e213-5.
Language English Country Great Britain, England Media print
Document type Letter, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid20064120
PubMed
20064120
DOI
10.1111/j.1755-3768.2009.01802.x
PII: AOS1802
Knihovny.cz E-resources
- MeSH
- Gene Amplification MeSH
- White People MeSH
- Genetic Diseases, X-Linked genetics MeSH
- Genotype MeSH
- Humans MeSH
- Microsatellite Repeats MeSH
- Molecular Biology MeSH
- Mutation genetics MeSH
- Eye Proteins genetics MeSH
- Polymerase Chain Reaction MeSH
- Retinitis Pigmentosa genetics MeSH
- Pedigree MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Eye Proteins MeSH
- RPGR protein, human MeSH Browser
References provided by Crossref.org
