Mutations in Cytokine Receptor-Like Factor 1 (CRLF1) Account for Both Crisponi and Cold-Induced Sweating Syndromes

This publication has 14 references indexed in Scilit:

• Cold-induced sweating syndrome A report of two cases and demonstration of genetic heterogeneity
  Journal of the Neurological Sciences, 2006
• Inactivation of cardiotrophin-like cytokine, a second ligand for ciliary neurotrophic factor receptor, leads to cold-induced sweating syndrome in a patient
  Proceedings of the National Academy of Sciences, 2006
• Neonatal paroxysmal trismus and camptodactyly: The Crisponi syndrome
  American Journal of Medical Genetics Part A, 2005
• Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome
  American Journal of Human Genetics, 2004
• Crisponi syndrome: Report of a further patient
  American Journal of Medical Genetics Part A, 2003
• Cold-Induced Sweating Syndrome Is Caused by Mutations in the CRLF1 Gene
  American Journal of Human Genetics, 2003
• The ciliary neurotrophic factor receptor alpha component induces the secretion of and is required for functional responses to cardiotrophin-like cytokine
  The EMBO Journal, 2001
• Suckling defect in mice lacking the soluble haemopoietin receptor NR6
  Current Biology, 1999
• Mice lacking the CNTF receptor, unlike mice lacking CNTF, exhibit profound motor neuron deficits at birth
  Cell, 1995
• A null mutation in the human CNTF gene is not causally related to neurological diseases
  Nature Genetics, 1994