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

1. Sarasola, E.
2. Rodríguez, J.A.
3. Garrote, E.
4. Arístegui, J.
5. García-Barcina, M.J.

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DOI: 10.1186/1471-2350-12-86 GOOGLE SCHOLAR lock_openOpen access editor

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