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Article

Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia

8 Aug 2015

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PMID: 26260707
DOI: 10.1016/j.ejmg.2015.08.001

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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 paraplegiaPMID 26260707Read ↗

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