Molecular aspects of pain research
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology,Genetics,Molecular Medicine
Link
http://www.nature.com/articles/6500095.pdf
Reference62 articles.
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3. Dawkins JL, Hulme DJ, Brahmbhatt SB, Auer-Grumbach M, Nicholson GA . Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I Nat Genet 2001 27: 309–312
4. Indo Y, Tsuruta M, Hayashida Y, Karim MA, Ohta K, Kawano T et al . Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis Nat Genet 1996 13: 485–488
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