A new case of infantile-onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family.

Eur J Neurol

Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation.

Published: May 2019

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http://dx.doi.org/10.1111/ene.13880	DOI Listing

Publication Analysis

case infantile-onset

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hereditary spastic

spastic paraplegia

paraplegia complicated

complicated phenotype

phenotype spg61

spg61 consanguineous

consanguineous russian

russian family

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