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Article

Association between SCO2 mutation and extreme myopia in Japanese patients.

Japanese journal of ophthalmology - 1 Jul 2016

Wakazono Tomotaka, Miyake Masahiro, Yamashiro Kenji, Yoshikawa Munemitsu, Yoshimura Nagahisa

Abstract excerpt

PURPOSE: To investigate the role of SCO2 in extreme myopia of Japanese patients. METHODS: In total, 101 Japanese patients with extreme myopia (axial length of ≥30 mm) OU at the Kyoto University Hospital were included in this study. Exon 2 of SCO2 was sequenced by conventional Sanger sequencing. The detected variants were assessed using in silico prediction programs: SIFT, PolyPhen-2 and MutationTaster. To...

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Identifiers

PMID: 27052445
DOI: 10.1007/s10384-016-0442-4

Genes

SCO2

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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