PubRank

Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype.

PubWeight™: 0.75‹?›

🔗 View Article (PMID 28626794)

Published in Neurol Genet on May 23, 2017

Authors

Rubina Dad1, Susan Walker1, Stephen W Scherer1, Muhammad Jawad Hassan1, Mohammad Domaia Alghamdi1, Berge A Minassian1, Reem A Alkhater1

Author Affiliations

1: Atta-ur Rahman School of Applied Biosciences (R.D., M.J.H.), National University of Sciences and Technology (NUST), Pakistan; Program in Genetics and Genome Biology (R.D., B.A.M.), Division of Neurology (B.A.M.), Department of Paediatrics, and The Centre for Applied Genomics, Genetics and Genome Biology (S.W., S.W.S.), The Hospital for Sick Children; Department of Molecular Genetics (S.W.S.), and McLaughlin Centre (S.W.S.), University of Toronto, Ontario, Canada; and Department of Pediatrics (M.D.A., R.A.A.), Division of Neurology, Johns Hopkins Aramco Healthcare, Dhahran, Saudi Arabia.

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