Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Abstract Background and objective Autosomal recessive genetic disorders pose significant health challenges in regions where consanguineous marriages are prevalent. The utilization of exome sequencing as a frequently employed methodology has enabled a clear delineation of diagnostic efficacy and mode...
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BMC,
2024-08-01T00:00:00Z.
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