Mašindová, Ivica <br/><br/>
MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.  [electronic resource] 

 -  PloS one  2015 
 - e0124232 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0124232  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Alleles<br/>Connexin 26<br/>Connexins<br/>Czech Republic--ethnology<br/>Exons--genetics<br/>Founder Effect<br/>Gene Frequency<br/>Genotype<br/>Haplotypes--genetics<br/>Hearing Loss--congenital<br/>Humans<br/>Hungary--ethnology<br/>Infant<br/>MARVEL Domain Containing 2 Protein--genetics<br/>Mutation<br/>Pakistan--ethnology<br/>Polymorphism, Single Nucleotide<br/>Prevalence<br/>Roma--genetics<br/>Sequence Homology, Nucleic Acid<br/>Slovakia--ethnology