Perry syndrome with a novel mutation and a rare presentation: First report from India
Conclusion: Perry syndrome, though rare, should be considered in the differential diagnosis of patients with a family history of Parkinsonism and central hypoventilation.
Source: Annals of Indian Academy of Neurology - Category: Neurology Authors: Pramod Krishnan Gosala R K. Sarma Uday Murgod Murali Srinivas Ajit K Roy Source Type: research
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