Kilquist Syndrome: A Novel Syndromic Hearing Loss Disorder Caused by Homozygous Deletion of SLC12A2.

Authors

Ellen F Macnamara
Alanna E Koehler
Precilla D'Souza
Tyra Estwick
Paul Lee
Gilbert Vezina, George Washington University
Harper Fauni
Stephen R Braddock
Erin Torti
James Matthew Holt
Prashant Sharma
May Christine V Malicdan
Cynthia J Tifft

Document Type

Journal Article

Publication Date

2-10-2019

Journal

Human mutation

DOI

10.1002/humu.23722

Comments

Epub ahead of print

APA Citation

Macnamara, E., Koehler, A., D'Souza, P., Estwick, T., Lee, P., Vezina, G., Fauni, H., Braddock, S., Torti, E., Holt, J., Sharma, P., Malicdan, M., & Tifft, C. (2019). Kilquist Syndrome: A Novel Syndromic Hearing Loss Disorder Caused by Homozygous Deletion of SLC12A2.. Human mutation, (). http://dx.doi.org/10.1002/humu.23722

Peer Reviewed

1