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. [electronic resource]

By: Contributor(s): Producer: 20110915Description: 86 p. digitalISSN:
  • 1471-2350
Subject(s): Online resources: In: BMC medical genetics vol. 12
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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