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Figure 1 | BMC Medical Genetics

Figure 1

From: 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

Figure 1

Pedigree of the family and results of the NTRK1 genetic analysis in CIPA patients' DNA. A. As indicated by the symbols in the pedigree, individual II-1 is affected by CIPA, whereas her parents and sister are all carriers. The NTRK1 mutation detected in each individual is indicated under the corresponding symbol. B. Electropherograms demonstrating the presence of two NTRK1 point mutations (in IVS5 and IVS16) in DNA from individual II-1. The position of each mutation is indicated by an asterisk.

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BMC Medical Genetics

ISSN: 1471-2350

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