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A Novel Missense Mutation in the TGF-β-binding Protein-Like Domain 3 of FBN1 Causes Weill–Marchesani Syndrome with Intellectual Disability

Author / Creator:Hassani, Mahdieh ; Taghizadeh, Sara ; Farahzad Broujeni, Anahita ; Habibi, Mahvash ; Banitalebi, Setareh ; Kasiri, Mahbubeh ; Sadeghi, Alireza ; Nozari, Ahoura

Publisher:India: Wolters Kluwer - Medknow

Journal title:Advanced biomedical research, 2023-01, Vol.12 (1), p.114-114

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A Novel Missense Mutation in the TGF-β-binding Protein-Like Domain 3 of FBN1 Causes Weill–Marchesani Syndrome with Intellectual Disability

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