A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.

No abstract is available for this paper.

• Publication year

  2014

• Venue

  Journal of Neurological Sciences

• Publication date

  2014-12-15

• Fields of study

  Medicine

• Identifiers
  DOI 10.1016/j.jns.2014.10.018PMID 25454649
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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