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pro vyhledávání: '"Ik Hyun Jeon"'
Autor:
Hye Ji Choi, Hyun Jae Lee, Jin Young Choi, Ik Hyun Jeon, Byunghwa Noh, Sushil Devkota, Han-Woong Lee, Seong Kug Eo, Jae Young Choi, Min Goo Lee, Jinsei Jung
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 188-197 (2020)
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 loss. Although the main pathological mechanism of H723R was identified as a p
Externí odkaz:
https://doaj.org/article/03023b2578ba4536a741af8aa7224e62
Autor:
Jae Young Choi, Byunghwa Noh, Seong Kug Eo, Hye Ji Choi, Sushil Devkota, Hyunjae Lee, Min Goo Lee, Jin Young Choi, Han Woong Lee, Ik Hyun Jeon, Jinsei Jung
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss, Pp 188-197 (2020)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
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 loss. Although the main pathological mechanism of H723R was identified as a p
Autor:
Sung Chul Lee, Suk Ho Byeon, Ik Hyun Jeon, Jeong H Bae, Christopher Seungkyu Lee, Hyoung Jun Koh
Publikováno v:
Retina. 30:1714-1720
Purpose: To report on the clinical features and the natural course of optic disk melanocytoma in the Korean population. Methods: A retrospective review of medical records was performed on 27 consecutive patients with optic disk melanocytoma. In cases