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

Metadata

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