Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss

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Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss

Author: Hofrichter, Michaela A. H.; Doll, Julia; Habibi, Haleh; Enayati, Samaneh; Mehrjardi, Mohammad Yahya Vahidi; Mueller, Tobias; Dittrich, Marcus; Haaf, Thomas; Vona, Barbara
Tübinger Autor(en):
Vona, Barbara
Published in: European Journal of Medical Genetics (2019), Bd. 62, Article UNSP 103724
Verlagsangabe: Elsevier
Language: English
Full text: http://dx.doi.org/10.1016/j.ejmg.2019.103724
ISSN: 1878-0849
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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