Localization of candidate regions for a novel gene for Kartagener syndrome

This publication has 25 references indexed in Scilit:

• Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
  Nature Genetics, 2003
• Missense Mutations in CRELD1 Are Associated with Cardiac Atrioventricular Septal Defects
  American Journal of Human Genetics, 2003
• Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD
  Journal of Medical Genetics, 2002
• Identification of Dynein Heavy Chain 7 as an Inner Arm Component of Human Cilia That Is Synthesized but Not Assembled in a Case of Primary Ciliary Dyskinesia
  Journal of Biological Chemistry, 2002
• Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry
  Nature Genetics, 2002
• Axonemal Dynein Intermediate-Chain Gene (DNAI1) Mutations Result in Situs Inversus and Primary Ciliary Dyskinesia (Kartagener Syndrome)
  American Journal of Human Genetics, 2001
• Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects
  Nature Genetics, 2000
• Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development
  American Journal of Human Genetics, 1999
• X-linked situs abnormalities result from mutations in ZIC3
  Nature Genetics, 1997
• Mutations of theConnexin43Gap-Junction Gene in Patients with Heart Malformations and Defects of Laterality
  New England Journal of Medicine, 1995