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Familial multiple pterygium syndrome (MPS) is not associated with CHRNG gene mutation

โœ Scribed by Paolo Prontera; Julie Vogt; Carole McKeown; Alberto Sensi


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
58 KB
Volume
143A
Category
Article
ISSN
1552-4825

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## Abstract Multiple system atrophy (MSA) is characterized clinically by Parkinsonism, cerebellar dysfunction, and autonomic impairment. Multiple mutations in the __LRRK2__ gene are associated with parkinsonian disorders, and the most common one, the G2019S mutation, has been found in โˆผ1% of sporad