Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature
Abstract Aim and Objective Intellectual disability (ID) is a heterogeneous condition affecting brain development, function, and/or structure. The X-linked mode of inheritance of ID (X-linked intellectual disability; XLID) has a prevalence of 1 out of 600 to 1000 males. In the last decades, exome seq...
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Main Authors: | Atefeh Mir (Author), Yongjun Song (Author), Hane Lee (Author), Hossein Khanahmad (Author), Erfan Khorram (Author), Jafar Nasiri (Author), Mohammad Amin Tabatabaiefar (Author) |
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Format: | Book |
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BMC,
2023-10-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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