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New compound heterozygous USH2A mutations in Usher syndrome
Author(s) -
Kuang Longhao,
Chen Qingshan,
Gan Run,
Yan Xiaohe
Publication year - 2020
Publication title -
acta ophthalmologica
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.534
H-Index - 87
eISSN - 1755-3768
pISSN - 1755-375X
DOI - 10.1111/aos.13969
Subject(s) - usher syndrome , retinitis pigmentosa , medicine , compound heterozygosity , hearing loss , audiology , ophthalmology , genetics , mutation , biology , retinal , gene
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