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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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A 28-year-old Woman with Lower Extremity Spasticity and Microcytic Anemia
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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X-Linked Pure Familial Spastic Paraparesis
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Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
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Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
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