Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186

Overview of attention for article published in Frontiers in Genetics, September 2019

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Biallelic NFASC #mutation https://t.co/GiiMtiHnsS linked t #ataxia https://t.co/soEdlVuJ9h

18 Oct 2019

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Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186. https://t.co/G67EBdcBm2

15 Oct 2019

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New Research: Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186: The etiology of hereditary ataxia syndromes is heterogeneous, and the mechanisms underlying these disorders are often unknown. Here, we utilized… https://t.c

30 Sep 2019

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Congratulations Bryndis on your newly published @FrontiersIn article: https://t.co/k0oq9merBH

24 Sep 2019

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