Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

No abstract is available for this paper.

• Publication year

  2013

• Venue

  Gene

• Publication date

  2013-10-10

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.gene.2013.06.040PMID 23845777
• 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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