Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.

Details

Language :

English

ISSN :

15524841

Volume :

171B

Issue :

6

Database :

Complementary Index

Journal :

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics

Publication Type :

Academic Journal

Accession number :

117418458

Full Text :

https://doi.org/10.1002/ajmg.b.32458