Publications by authors named "Anna Pryde"

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Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.
Michael A Simpson, Harold Cross, Christos Proukakis, David A Priestman, David C A Neville, Anna Pryde

Nat Genet· November 2004

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Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia.
Michael A Simpson, Harold Cross, Christos Proukakis, Anna Pryde, Ruth Hershberger

Am J Hum Genet· November 2003

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