Literature DB >> 12406349

The M581V mutation, associated with a mild form of congenital insensitivity to pain with anhidrosis, causes partial inactivation of the NTRK1 receptor.

Claudia Miranda, Silvia Selleri, Marco A Pierotti, Angela Greco.   

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Year:  2002        PMID： 12406349     DOI： 10.1046/j.1523-1747.2002.00140.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  2 in total

Review 1.  Pain and stress in a systems perspective: reciprocal neural, endocrine, and immune interactions.

Authors:  C Richard Chapman; Robert P Tuckett; Chan Woo Song
Journal:  J Pain       Date:  2007-12-21       Impact factor: 5.820

2.  A short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis.

Authors:  Esther Sarasola; Jose A Rodríguez; Elisa Garrote; Javier Arístegui; Maria J García-Barcina
Journal:  BMC Med Genet       Date:  2011-06-27       Impact factor: 2.103
  2 in total

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