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Article

Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families

4 Jul 2019

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31281085
DOI: 10.1016/j.jocn.2019.06.039

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Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani familiesPMID 31281085Read ↗

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Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegiaSemantic proximity Read ↗

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