PRUNE1
收藏NIAID Data Ecosystem2026-03-13 收录
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资源简介：
By whole-exome sequencing, we identified the start loss variant, M_021222.3:c.3G>A; p.(Met1?), in the PRUNE1 in two patients of a consanguineous Iranian family with spastic quadriplegic cerebral palsy (CP), hypotonia, developmental regression, and cerebellar atrophy.
创建时间：
2022-02-12
