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

Eur J Neurol. 2019 May;26(5):e61-e62. doi: 10.1111/ene.13880.

Authors

A L Chukhrova¹, I A Akimova¹, O A Shchagina¹, V A Kadnikova¹, O P Ryzhkova¹, A V Polyakov¹

Affiliation

¹ Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russian Federation.

PMID: 30980493
DOI: 10.1111/ene.13880

No abstract available

Keywords: ARL6IP1; SPG61; consanguineous; hereditary spastic paraplegia; homozygosity; whole-exome sequencing.

Publication types

Letter