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Reply to: Fatal Familial Insomnia: A Rare Disease with Unique Clinico- Neurophysiological Features

Movement disorders clinical practice, Vol. 8, Issue 1, Pages 164-165, 2020

PMID: 33426176

Baldelli et al. 1 raise an important issue in respect to our report of a 54 year old man with D178N mutation in PRNP gene presenting with rapidly progressive autosomal dominant ataxia and vocal cord palsy.

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  https://www.ncbi.nlm.nih.gov/pubmed/33426176

 

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