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

Internet

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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