The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene
Open Access
- 10 February 1995
- Vol. 25 (3) , 730-732
- https://doi.org/10.1016/0888-7543(95)80019-i
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomePublished by Elsevier ,2004
- CEPH Consortium Map of Chromosome 9Genomics, 1994
- Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisNature Genetics, 1993
- Similarities and differences in the way neurotrophins interact with the Trk receptors in neuronal and nonneuronal cellsNeuron, 1993
- Neurotrophin receptors: A window into neuronal differentiationNeuron, 1992
- The trk B tyrosine protein kinase is a receptor for neurotrophin-4Neuron, 1992
- Mammalian neurotrophin-4: structure, chromosomal localization, tissue distribution, and receptor specificity.Proceedings of the National Academy of Sciences, 1992
- Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.Proceedings of the National Academy of Sciences, 1991
- A genetic linkage map of the human genomeCell, 1987
- FAMILIAL DYSAUTONOMIAMedicine, 1970