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
- Sarasola, E.
- Rodríguez, J.A.
- Garrote, E.
- Arístegui, J.
- García-Barcina, M.J.
Revue:
BMC Medical Genetics
ISSN: 1471-2350
Année de publication: 2011
Volumen: 12
Type: Article
