Cerebellar cognitive affective syndrome: insights from Joubert syndrome
Abstract Background Joubert syndrome (JS) is a rare, autosomal recessively inherited genetic disorder characterized morphologically by unique developmental malformations of the cerebellum and brainstem (the molar tooth sign), and clinically by impaired motor functions and intellectual disability. Pa...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-03-01
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Series: | Cerebellum & Ataxias |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40673-018-0085-y |