Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype.

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Parkinsonism & Related Disorders

• Publication date

  2016-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.parkreldis.2015.12.012PMID 26725140
• 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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