A splice-site variant (c.3289-1G>T) in OTOF underlies profound hearing loss in a Pakistani kindred
收藏NIAID Data Ecosystem2026-03-12 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP292357
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资源简介：
The splicing variants of OTOF (NM_194248, c.3289-1G>T) cosegregated with the disease phenotype in this Pakistani family
创建时间：
2020-11-18
