Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy

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Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy

Author: Shaikh, Rehan S.; Reuter, Peggy; Sisk, Robert A.; Kausar, Tasleem; Shahzad, Mohsin; Maqsood, Muhammad I.; Yousif, Ateeq; Ali, Muhammad; Riazuddin, Saima; Wissinger, Bernd; Ahmed, Zubair M.
Tübinger Autor(en):
Reuter, Peggy
Wissinger, Bernd
Published in: European Journal of Human Genetics (2015), Bd. 23, H. 4, S. 473-480
Verlagsangabe: Nature Publishing Group
Language: English
Full text: http://dx.doi.org/10.1038/ejhg.2014.136
ISSN: 1018-4813
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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