SPTLC1 is mutated in hereditary sensory neuropathy, type 1
Nature Genetics2001Vol. 27(3), pp. 261–262
Citations Over TimeTop 10% of 2001 papers
Khemissa Bejaoui, Chenyan Wu, Margaret Scheffler, Geoffry Haan, P. Ashby, Lianchan Wu, Peter J. de Jong, Robert H. Brown
Related Papers
- → Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer(1998)66 cited
- → The effects of sensory interaction and sensory conflict on consumer online review rating behavior(2023)4 cited
- → Synaptic connections between different sensory channels in CNS of the leech modulate the input of mechanosensory information(1998)
- → Amplification of c-myc Locus is Independently Associated with the Deletions of Chromosome 8p in Breast Carcinoma(2005)
- → World distribution of carbonic anhydrase variants(1980)