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Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.
Volume 63 (2009): Numero 4-5 (October 2009)
Accesso libero
Spectrum and Frequency of the
GJB2
Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss
Olga Šterna
Olga Šterna
,
Natālija Proņina
Natālija Proņina
,
Ieva Grīnfelde
Ieva Grīnfelde
,
Sandra Kušķe
Sandra Kušķe
,
Astrīda Krūmiņa
Astrīda Krūmiņa
,
Rita Lugovska
Rita Lugovska
e
Aigars Pētersons
Aigars Pētersons
| 06 nov 2009
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.
Volume 63 (2009): Numero 4-5 (October 2009)
The National Research Programme On Main Diseases Threatening The Life Expectancy and Life Quality of The Latvian Population: Scientific papers
INFORMAZIONI SU QUESTO ARTICOLO
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CONDIVIDI
Pubblicato online:
06 nov 2009
Pagine:
198 - 203
DOI:
https://doi.org/10.2478/v10046-009-0031-8
Parole chiave
hearing loss
,
GJB2
,
connexon
,
gap junction
,
DFNB1 - deafness autosomal recessive type 1
This content is open access.
Olga Šterna
Clinic of Medical Genetics, Children's Clinical University Hospital, Juglas iela 20, Rga, LV-1079, LATVIA
Natālija Proņina
Clinic of Medical Genetics, Children's Clinical University Hospital, Juglas iela 20, Rga, LV-1079, LATVIA
Ieva Grīnfelde
Clinic of Medical Genetics, Children's Clinical University Hospital, Juglas iela 20, Rga, LV-1079, LATVIA
Sandra Kušķe
Centre for Hearing Impaired Children of Latvia, Lielvārdes iela 68/1, Rga, LV-1006, LATVIA
Astrīda Krūmiņa
Rga Stradiņš University, Dzirciema iela 16, Rga, LV-1007, LATVIA
Rita Lugovska
Clinic of Medical Genetics, Children's Clinical University Hospital, Juglas iela 20, Rga, LV-1079, LATVIA
Aigars Pētersons
Rga Stradiņš University, Dzirciema iela 16, Rga, LV-1007, LATVIA