ARSACS as a Worldwide Disease: Novel SACS Mutations Identified in a Consanguineous Family from the Remote Tribal Jammu and Kashmir Region in India

Overview of attention for article published in The Cerebellum, April 2019

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RT @varsome: Novel SACS #mutations https://t.co/exp1lwgeqt identified in #Indian consanguineous family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) neurodegenerative disorder #neurology #raredisease https://t.co/xXZ0ta3Blo

Novel SACS #mutations https://t.co/n3kFS0yEyt identified in #Indian consanguineous family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) neurodegenerative disorder #neurology #raredisease https://t.co/hiCEu3ObZW

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