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                                       Details for article 42 of 88 found articles
 
 
  Homozygous frameshift mutation of SPG11 as a cause of progressive flaccid paralysis, ataxia and dysphagia
 
 
Title: Homozygous frameshift mutation of SPG11 as a cause of progressive flaccid paralysis, ataxia and dysphagia
Author: Lilley, Kate
Bhuta, Sandeep
Sabet, Arman
Broadley, Simon A
Appeared in: Journal of clinical neuroscience
Paging: Volume 81 () nr. C pages 90-91
Year: 2020
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 42 of 88 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands