Can mutations in the ribosomal protein S26 (RPS26) gene lead to Klippel-Feil syndrome in Diamond-Blackfan anemia patients? An update from the Czech Diamond-Blackfan Anemia registry
Blood cells, molecules & diseases.
2011 Apr 15 ;
46 (4) :
300-1.
Language English Country United States Media print
Document type Letter, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid21414820
PubMed
21414820
DOI
10.1016/j.bcmd.2011.02.003
PII: S1079-9796(11)00031-3
Knihovny.cz E-resources
- MeSH
- Anemia, Diamond-Blackfan complications genetics MeSH
- Klippel-Feil Syndrome etiology genetics MeSH
- Humans MeSH
- Mutation MeSH
- Registries MeSH
- Ribosomal Proteins genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Names of Substances
- Ribosomal Proteins MeSH
- RPS26 protein, human MeSH Browser
References provided by Crossref.org
