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Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

Detalles Bibliográficos
Autores principales: Lee, Yun Jeong, Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Ophthalmological Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105792/
https://www.ncbi.nlm.nih.gov/pubmed/32233153
http://dx.doi.org/10.3341/kjo.2019.0080
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author Lee, Yun Jeong
Joo, Kwangsic
Seong, Moon-Woo
Park, Kyu Hyung
Park, Sung Sup
Woo, Se Joon
author_facet Lee, Yun Jeong
Joo, Kwangsic
Seong, Moon-Woo
Park, Kyu Hyung
Park, Sung Sup
Woo, Se Joon
author_sort Lee, Yun Jeong
collection PubMed
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spelling pubmed-71057922020-04-09 Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient Lee, Yun Jeong Joo, Kwangsic Seong, Moon-Woo Park, Kyu Hyung Park, Sung Sup Woo, Se Joon Korean J Ophthalmol Correspondence The Korean Ophthalmological Society 2020-04 2020-03-16 /pmc/articles/PMC7105792/ /pubmed/32233153 http://dx.doi.org/10.3341/kjo.2019.0080 Text en © 2020 The Korean Ophthalmological Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Correspondence
Lee, Yun Jeong
Joo, Kwangsic
Seong, Moon-Woo
Park, Kyu Hyung
Park, Sung Sup
Woo, Se Joon
Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title_full Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title_fullStr Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title_full_unstemmed Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title_short Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient
title_sort congenital stationary night blindness due to novel trpm1 gene mutations in a korean patient
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105792/
https://www.ncbi.nlm.nih.gov/pubmed/32233153
http://dx.doi.org/10.3341/kjo.2019.0080
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