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Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening
Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening
2017
Channa Hewamadduma
R. Omalley
M.H. Robinson
N Beauchamp
T. Rogers
Joanne Martindale
Christopher J. McDermott
Pamela J. Shaw
Nigel Hoggard
M. Hadjivassiliou
Keywords:
Cohort
Diabetes mellitus
Pediatrics
Phenotype
Physical therapy
Spastic ataxia
Medicine
Correction
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