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Article

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

Journal of neurology - 1 Sept 2017

Scarlato Marina, Citterio Andrea, Barbieri Alessandra, Godi Claudia, Panzeri Elena, Bassi Maria Teresa

Abstract excerpt

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Topics

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Share to Adaptor Proteins, Signal Transducing
Share to Brain
Share to Dementia
Share to Exome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Homozygote

Share to Sequence Analysis, DNA

Share to Spastic Paraplegia, Hereditary

Source

Identifiers

PMID: 28752238
DOI: 10.1007/s00415-017-8558-0

Genes

SPG21

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.PMID 28752238Read ↗

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