Amanda Krause to Spinocerebellar Ataxias
This is a "connection" page, showing publications Amanda Krause has written about Spinocerebellar Ataxias.
Connection Strength
0,660
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A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci. J Neurol Sci. 2018 07 15; 390:200-204.
Score: 0,604
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The hereditary adult-onset ataxias in South Africa. J Neurol Sci. 2003 Dec 15; 216(1):47-54.
Score: 0,056