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Publications by M. T. Littleton-Kearney
Hereditary Spastic Paraplegia and Amyotrophy Associated With a Novel Locus on Chromosome 19
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
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A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3
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A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-Q34
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Hereditary Ataxia and Spastic Paraplegia in Portugal
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Hereditary Spastic Paraplegia Type 8 - Neuropathological Findings
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Protrudin Regulates Endoplasmic Reticulum Morphology and Function Associated With the Pathogenesis of Hereditary Spastic Paraplegia
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Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia
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Autosomal Dominant Hereditary Spastic Paraplegia: Novel Mutations in the REEP1 Gene (SPG31)
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