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

por Hassani, Mahdieh, Taghizadeh, Sara, Farahzad Broujeni, Anahita, Habibi, Mahvash, Banitalebi, Setareh, Kasiri, Mahbubeh, Sadeghi, Alireza, Nozari, Ahoura
Publicado 2023