Novel ophthalmic abnormalities in two individuals with a homozygous p.W185* mutation in C8orf37 and Bardet-Biedl syndrome
收藏NIAID Data Ecosystem2026-03-14 收录
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资源简介：
Whole genome sequencing of a familiy with Bardet-Biedl syndrome
创建时间：
2023-03-23
