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Article

Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia.

Clinical genetics - 1 Apr 2014

Donkervoort S, Dastgir J, Hu Y, Zein W M, Marks H, Blackstone C, Bönnemann C G

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23745665
DOI: 10.1111/cge.12185
PMCID: PMC5030767

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