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Genet Med. 2019 Oct;21(10):2409. doi: 10.1038/s41436-019-0553-7.

Correction: ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

Author information

1
Laboratory for Molecular Medicine, Partners Healthcare Personalized Medicine, Cambridge, MA, USA.
2
The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
3
Dept. of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, MA, USA.
4
Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of Iowa Hospital and Clinics, Iowa City, IA, USA.
5
The Interdisciplinary Graduate Program in Molecular Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
6
ARUP Laboratories, Salt Lake City, UT, USA.
7
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
8
Division of Hearing and Balance Research, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
9
Medical Genetics Center, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
10
Harvard Medical School, Boston, MA, USA.
11
The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
12
Department of Otorhinolaryngology, Clinical Genomics and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
13
John P. Hussman Institute for Human Genomics, University of Miami, Miami, FL, USA.
14
Al Jalila Children's Specialty Hospital, Al Jaddaf, Dubai, United Arab Emirates.
15
Laboratory for Molecular Medicine, Partners Healthcare Personalized Medicine, Cambridge, MA, USA. samr@partners.org.
16
Harvard Medical School, Boston, MA, USA. samr@partners.org.

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

PMID:
31114025
DOI:
10.1038/s41436-019-0553-7

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