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1. A case of Friedreich ataxia in an adolescent with 16p11.2 microdeletion syndrome.

Author

Pelliccia V, Ferranti S, Mostardini R, and Grosso S

Subjects
Adolescent, Autistic Disorder complications, Chromosome Deletion, Chromosome Disorders complications, Chromosomes, Human, Pair 16, Developmental Disabilities etiology, Friedreich Ataxia etiology, Humans, Intellectual Disability complications, Male, Autistic Disorder diagnosis, Chromosome Disorders diagnosis, Developmental Disabilities diagnosis, Friedreich Ataxia diagnosis, Intellectual Disability diagnosis
Published
2020
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