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Article

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

Korean journal of ophthalmology : KJO - 1 Apr 2020

Lee Yun Jeong, Joo Kwangsic, Seong Moon Woo, Park Kyu Hyung, Park Sung Sup, Woo Se Joon

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Share to Electroretinography
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32233153
DOI: 10.3341/kjo.2019.0080
PMCID: PMC7105792

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Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient.PMID 32233153Read ↗

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