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Neurodevelopmental Disorder with Eye Movement Abnormalities and Ataxia
An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy and that is caused by heterozygous mutation in the FRMD5 gene on chromosome 15q15. Affec
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Overview
An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy and that is caused by heterozygous mutation in the FRMD5 gene on chromosome 15q15. Affec
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