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

Chukhrova, A L; Akimova, I A; Shchagina, O A; Kadnikova, V A; Ryzhkova, O P; Polyakov, A V.

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.

Eur J Neurol ; 26(5): e61-e62, 2019 05.

Article en En | MEDLINE | ID: mdl-30980493