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Article

A novel frameshift DDHD1 mutation in a patient with hereditary spastic paraplegia type 28: Case report and review of the literature.

Parkinsonism & related disorders - 1 Jan 2024

Pinheiro Rita Gonçalo, Leal Rato Miguel, Silva Cláudia Santos, Soares Marta P, Carvalho Vanessa, Guedes Leonor Correia

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 37984267
DOI: 10.1016/j.parkreldis.2023.105931

Genes

DDHD1

Provenance

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

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