MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin. [electronic resource]
Producer: 20160412Description: e0124232 p. digitalISSN:- 1932-6203
- 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
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Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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