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Article

Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype.

Journal of neurology - 1 Jun 2008

Haberlová J, Claeys K G, Zámecník J, De Jonghe P, Seeman P

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18446315
DOI: 10.1007/s00415-008-0598-z

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Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype.PMID 18446315Read ↗

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Patients with complex and very-early-onset ATL1-related spastic paraplegia offer insights on genotype/phenotype correlations and support for autosomal recessive forms of SPG3A.Semantic proximity Read ↗

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