CNGB3 mutations cause severe rod dysfunction

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CNGB3 mutations cause severe rod dysfunction

Author: Maguire, J.; McKibbin, M.; Khan, K.; Kohl, S.; Ali, M.; McKeefry, D.
Tübinger Autor(en):
Kohl, Susanne
Published in: Ophthalmic Genetics (2018), Bd. 39, H. 1, S. 108-114
Verlagsangabe: Taylor & Francis Inc
Language: English
Full text: http://dx.doi.org/10.1080/13816810.2017.1368087
ISSN: 1744-5094
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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