A homozygous stop gain mutation in BOD1 gene in a Lebanese patient with syndromic intellectual disability.

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Source: Clinical Genetics - June 23, 2020 Category: Genetics & Stem Cells Authors: Hamdan N, Mehawej C, Sebaaly G, Jalkh N, Corbani S, Abou-Ghoch J, De Backer O, Chouery E Tags: Clin Genet Source Type: research