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

Autor:	Chukhrova AL; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation., Akimova IA; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation., Shchagina OA; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation., Kadnikova VA; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation., Ryzhkova OP; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation., Polyakov AV; Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation.
Jazyk:	angličtina
Zdroj:	European journal of neurology [Eur J Neurol] 2019 May; Vol. 26 (5), pp. e61-e62.
DOI:	10.1111/ene.13880
Databáze:	MEDLINE
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