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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:	Correspondence
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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