MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.
Mašindová, Ivica
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
Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0124232 doi
Age of Onset
Alleles
Connexin 26
Connexins
Czech Republic--ethnology
Exons--genetics
Founder Effect
Gene Frequency
Genotype
Haplotypes--genetics
Hearing Loss--congenital
Humans
Hungary--ethnology
Infant
MARVEL Domain Containing 2 Protein--genetics
Mutation
Pakistan--ethnology
Polymorphism, Single Nucleotide
Prevalence
Roma--genetics
Sequence Homology, Nucleic Acid
Slovakia--ethnology
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
Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0124232 doi
Age of Onset
Alleles
Connexin 26
Connexins
Czech Republic--ethnology
Exons--genetics
Founder Effect
Gene Frequency
Genotype
Haplotypes--genetics
Hearing Loss--congenital
Humans
Hungary--ethnology
Infant
MARVEL Domain Containing 2 Protein--genetics
Mutation
Pakistan--ethnology
Polymorphism, Single Nucleotide
Prevalence
Roma--genetics
Sequence Homology, Nucleic Acid
Slovakia--ethnology