Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. uri icon

authors

  • McDonald-McGinn, Donna M
  • Bilaniuk, Larissa T
  • Sullivan, Kathleen E
  • Warren, Stephen T
  • Emanuel, Beverly S
  • Vermeesch, Joris R
  • Zackai, Elaine H
  • Jerome-Majewska, Loydie A
  • Fahiminiya, Somayyeh
  • Revil, Timothée
  • Nowakowska, Beata A
  • Suhl, Joshua
  • Bailey, Alice
  • Mlynarski, Elisabeth
  • David Lynch, MD, PhD
  • Yan, Albert C

publication date

  • January 1, 2012