LOXL3, encoding lysyl oxidase-like 3, is mutated in a family with autosomal recessive Stickler syndrome

No abstract is available for this paper.

• Publication year

  2015

• Venue

  Human Genetics

• Publication date

  2015-02-07

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00439-015-1531-zPMID 25663169
• 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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