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Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

Erstveröffentlichung
2011
Authors
Borck, Guntram
Rehman, Atteeq Ur
Lee, Kwanghyuk
Pogoda, Hans-Martin
Kakar, Naseebullah
et al.
Wissenschaftlicher Artikel


Published in
American journal of human genetics ; 88 (2011), 2. - S. 127-137. - ISSN 0002-9297
Link to publication
https://dx.doi.org/10.1016/j.ajhg.2010.12.011
Institutions
UKU. Institut für Humangenetik
Subject headings
[Free subject headings]: STIMULATED LIPOPROTEIN RECEPTOR | LINKAGE ANALYSIS | MOUSE MODELS | HAIR-CELLS | INNER-EAR | DEAFNESS | ZEBRAFISH | MICE | IDENTIFICATION | HYPERLIPIDEMIA
[DDC subject group]: DDC 570 / Life sciences

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