Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability - Archive ouverte HAL
Journal Articles Journal of Medical Genetics Year : 2024

Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability

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Biochemistry, Molecular Biology
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Submitted on : Monday, September 16, 2024-11:00:54 PM

Last modification on : Thursday, September 26, 2024-2:15:22 PM

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hal-04699527 , version 1 (16-09-2024)

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Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, et al.. Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of Medical Genetics, 2024, 61 (7), pp.689-698. ⟨10.1136/jmg-2023-109728⟩. ⟨hal-04699527⟩

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