Article

Autosomal dominant multiple pterygium syndrome is caused by mutations in MYH3

· 2015 · Chong JX, Burrage LC, Beck AE, Marvin CT, McMillin MJ, Shively KM, Buckingham KJ, Bacino CA, Jain M, Alanay Y, Berry SA, Carey JC, Gibbs RA, Lee BH, Krakow D, Shendure J, Nickerson DA, Center Mendelian Genomics UW, Bamshad MJ.

Key facts

Title Autosomal dominant multiple pterygium syndrome is caused by mutations in MYH3
First author Chong JX, Burrage LC, Beck AE, Marvin CT, McMillin MJ, Shively KM, Buckingham KJ, Bacino CA, Jain M, Alanay Y, Berry SA, Carey JC, Gibbs RA, Lee BH, Krakow D, Shendure J, Nickerson DA, Center Mendelian Genomics UW, Bamshad MJ.
Published Apr 3, 2015
DOI 10.1101/017434
Devices mentioned 017434

At a glance

  • 1–9 FDA submissions mentioned
  • None Product codes mentioned

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Literature

Peer-reviewed and preprint literature indexed by Orca1 and linked to the FDA submissions and product codes each article mentions. Only bibliographic details are shown here.

Source: Publisher and PubMed metadata; device mentions identified by Orca1

Browse all Literature