MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

Rad, A MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). Journal of Medical Genetics:-.

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Item Type: Article
Subjects: R Medicine > R Medicine (General)
Depositing User: mrs maryam koohestani
Date Deposited: 09 Sep 2026 04:59
Last Modified: 09 Sep 2026 04:59
URI: http://eprints.medsab.ac.ir/id/eprint/1099

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