A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy

No abstract is available for this paper.

• Publication year

  2000

• Venue

  Neurology

• Publication date

  2000-12-12

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1212/WNL.55.11.1689PMID 11113224
• 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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