Genomics

Dataset Information

0

Homo sapiens


ABSTRACT: Clinically Relevant Copy Number Variations Detected in Cerebral Palsy

ORGANISM(S): Homo sapiens  

PROVIDER: PRJNA288569 | ENA |

REPOSITORIES: ENA

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Publications


Cerebral palsy (CP) represents a group of non-progressive clinically heterogeneous disorders that are characterized by motor impairment and early age of onset, frequently accompanied by co-morbidities. The cause of CP has historically been attributed to environmental stressors resulting in brain damage. While genetic risk factors are also implicated, guidelines for diagnostic assessment of CP do not recommend for routine genetic testing. Given numerous reports of aetiologic copy number variation  ...[more]

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