[HTML][HTML] DNAJC14 ameliorates inner ear degeneration in the DFNB4 mouse model

HJ Choi, HJ Lee, JY Choi, IH Jeon, B Noh… - … Therapy-Methods & …, 2020 - cell.com
The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most prevalent
mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic hearing …

DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model.

HJ Choi, HJ Lee, JY Choi, IH Jeon, B Noh… - … therapy. Methods & …, 2019 - europepmc.org
Abstract The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most
prevalent mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic …

[HTML][HTML] DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model

HJ Choi, HJ Lee, JY Choi, IH Jeon, B Noh… - … Therapy-Methods & …, 2020 - Elsevier
The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most prevalent
mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic hearing …

DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model

HJ Choi, HJ Lee, JY Choi, IH Jeon… - Molecular Therapy …, 2020 - yonsei.elsevierpure.com
Abstract The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most
prevalent mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic …

[PDF][PDF] DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model

HJ Choi, HJ Lee, JY Choi, IH Jeon, B Noh… - Molecular …, 2020 - scienceopen.com
The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most prevalent
mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic hearing …

DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model

HJ Choi, HJ Lee, JY Choi, IH Jeon… - … therapy. Methods & …, 2019 - pubmed.ncbi.nlm.nih.gov
The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most prevalent
mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic hearing …

[HTML][HTML] DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model

HJ Choi, HJ Lee, JY Choi, IH Jeon, B Noh… - … Therapy. Methods & …, 2020 - ncbi.nlm.nih.gov
Abstract The His723Arg (H723R) mutation in SLC26A4, encoding pendrin, is the most
prevalent mutation in East Asia, resulting in DFNB4, an autosomal recessive type of genetic …