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Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss Cover

Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss

Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.
Volume 63 (2009): Issue 4-5 (October 2009)
By: ,  ,  ,  ,  ,   and    
Open Access
|Nov 2009
Authors

Authors

Olga Šterna

Natālija Proņina

Ieva Grīnfelde

Sandra Kušķe

Astrīda Krūmiņa

Rita Lugovska

Aigars Pētersons

DOI: https://doi.org/10.2478/v10046-009-0031-8 | Journal eISSN: 2255-890X | Journal ISSN: 1407-009X
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Language: English
Page range: 198 - 203
Published on: Nov 6, 2009
Published by: Latvian Academy of Sciences
In partnership with: Paradigm Publishing Services
Keywords:
hearing loss,
GJB2,
connexon,
gap junction,
DFNB1 - deafness autosomal recessive type 1
Related subjects:
General interest,
Mathematics,
General mathematics

© 2009 Olga Šterna, Natālija Proņina, Ieva Grīnfelde, Sandra Kušķe, Astrīda Krūmiņa, Rita Lugovska, Aigars Pētersons, published by Latvian Academy of Sciences
This work is licensed under the Creative Commons License.

Volume 63 (2009): Issue 4-5 (October 2009)