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Retinitis pigmentosa and deafness as a result of novel Leu130Pro mutation in PRPH2 gene and most common homozygous deletion 35delG in Gjb2 gene; differential diagnosis of Usher syndomeFakin, Ana ...Source: Molekularna medicina in biotehnologija = Molecular medicine and biotechnology : book of abstracts (Str. 68)Type of material - conference contributionPublish date - 2012Language - englishCOBISS.SI-ID - 29999833
Author
Fakin, Ana |
Zupan, Andrej, 1981- |
Glavač, Damjan |
Hawlina, Marko
Topics
Usher syndrome |
retinitis pigmentosa |
ophthalmologic
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DRS, in which the journal is indexed
Database name | Field | Year |
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Links to authors' personal bibliographies | Links to information on researchers in the SICRIS system |
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Fakin, Ana | 33340 |
Zupan, Andrej, 1981- | 28143 |
Glavač, Damjan | 09275 |
Hawlina, Marko | 09154 |
Source: Personal bibliographies
and: SICRIS
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