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J.NMD.2007.10.005
J.NMD.2007.10.005
http://dx.doi.org/10.1016/J.NMD.2007.10.005
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.
P356
Q40432173-23D7211D-02EE-4635-8BD3-18CB289C2A8D
P356
J.NMD.2007.10.005
http://dx.doi.org/10.1016/J.NMD.2007.10.005