Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA (NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor
- 1 June 1999
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 64 (6), 1570-1579
- https://doi.org/10.1086/302422
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain α-keto acid dehydrogenase complexJournal of Human Genetics, 1998
- Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosisNature Genetics, 1996
- Functional Interactions of Neurotrophins and Neurotrophin ReceptorsAnnual Review of Neuroscience, 1995
- Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)Genomics, 1995
- Functions of the neurotrophins during nervous system development: What the knockouts are teaching usCell, 1994
- Trk receptors use redundant signal transduction pathways involving SHC and PLC-γ1 to mediate NGF responsesNeuron, 1994
- The trk Proto-Oncogene Product: a Signal Transducing Receptor for Nerve Growth FactorScience, 1991
- The trk proto-oncogene encodes a receptor for nerve growth factorCell, 1991
- Expression of the trk proto-oncogene is restricted to the sensory cranial and spinal ganglia of neural crest origin in mouse development.Genes & Development, 1990
- Congenital insensitivity to pain with anhidrosisMuscle & Nerve, 1980