Ontology highlight
ABSTRACT:
SUBMITTER: Oishi A
PROVIDER: S-EPMC8624169 | biostudies-literature | 2021 Nov
REPOSITORIES: biostudies-literature
Oishi Akio A Fujinami Kaoru K Mawatari Go G Naoi Nobuhisa N Ikeda Yasuhiro Y Ueno Shinji S Kuniyoshi Kazuki K Hayashi Takaaki T Kondo Hiroyuki H Mizota Atsushi A Shinoda Kei K Kusuhara Sentaro S Nakamura Makoto M Iwata Takeshi T Tsujikawa Akitaka A Tsunoda Kazushige K
Genes 20211118 11
<i>Peripherin-2</i> (<i>PRPH2</i>) is one of the causative genes of inherited retinal dystrophy. While the gene is relatively common in Caucasians, reports from Asian ethnicities are limited. In the present study, we report 40 Japanese patients from 30 families with <i>PRPH2</i>-associated retinal dystrophy. We identified 17 distinct pathogenic or likely pathogenic variants using next-generation sequencing. Variants p.R142W and p.V200E were relatively common in the cohort. The age of onset was g ...[more]