An update on phosphodiesterase mutations underlying genetic etiology of hearing loss and retinitis pigmentosa

Rahul Mittal; Nicole Bencie; James M. Parrish; George Liu; Jeenu Mittal; Denise Yan; Xue Zhong Liu

doi:10.3389/fgene.2018.00009

An update on phosphodiesterase mutations underlying genetic etiology of hearing loss and retinitis pigmentosa

Rahul Mittal, Nicole Bencie, James M. Parrish, George Liu, Jeenu Mittal, Denise Yan, Xue Zhong Liu

Otolaryngology

Research output: Contribution to journal › Comment/debate

1 Scopus citations

Original language	English (US)
Article number	9
Journal	Frontiers in Genetics
Volume	9
Issue number	FEB
DOIs	https://doi.org/10.3389/fgene.2018.00009
State	Published - Feb 8 2018

Keywords

CRISPR/Cas9
Genetics
Hearing loss
Phosphodiesterase
Retinitis pigmentosa
Usher syndrome

ASJC Scopus subject areas

Molecular Medicine
Genetics
Genetics(clinical)

Access to Document

10.3389/fgene.2018.00009

Cite this

Mittal, R., Bencie, N., Parrish, J. M., Liu, G., Mittal, J., Yan, D., & Liu, X. Z. (2018). An update on phosphodiesterase mutations underlying genetic etiology of hearing loss and retinitis pigmentosa. Frontiers in Genetics, 9(FEB), [9]. https://doi.org/10.3389/fgene.2018.00009

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