MYO7A mutation screening in Usher syndrome type I patients from diverse origins
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
17361009
PubMed Central
PMC2598023
DOI
10.1136/jmg.2006.045377
PII: 44/3/e71
Knihovny.cz E-zdroje
- MeSH
- bodová mutace MeSH
- dyneiny genetika MeSH
- inzerční mutageneze MeSH
- lidé MeSH
- missense mutace MeSH
- místa sestřihu RNA genetika MeSH
- molekulární sekvence - údaje MeSH
- mutace * MeSH
- mutační analýza DNA MeSH
- myosin VIIa MeSH
- myosiny genetika MeSH
- nesmyslný kodon MeSH
- polymorfismus konformace jednovláknové DNA MeSH
- rodokmen MeSH
- sekvence aminokyselin MeSH
- sekvenční delece MeSH
- sekvenční homologie aminokyselin MeSH
- sekvenční seřazení MeSH
- tandemové repetitivní sekvence MeSH
- Usherovy syndromy etnologie genetika MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Geografické názvy
- Česká republika etnologie MeSH
- Itálie etnologie MeSH
- Maroko etnologie MeSH
- Španělsko etnologie MeSH
- Turecko etnologie MeSH
- Názvy látek
- dyneiny MeSH
- místa sestřihu RNA MeSH
- MYO7A protein, human MeSH Prohlížeč
- myosin VIIa MeSH
- myosiny MeSH
- nesmyslný kodon MeSH
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