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Neurodevelopmental Disorder with Motor and Language Delay, Ocular Defects, and Brain Abnormalities
An autosomal recessive intellectual developmental disorder that is characterized by the onset of features in infancy or early childhood and that is caused by homozygous or compound heterozygous mutation in the INTS11 gen
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Overview
An autosomal recessive intellectual developmental disorder that is characterized by the onset of features in infancy or early childhood and that is caused by homozygous or compound heterozygous mutation in the INTS11 gen
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