Condition: Obesity, Hyperphagia, and Developmental Delay
rs1554774973
in
NTRK2
gene and
Obesity, Hyperphagia, and Developmental Delay
PMID 27884935
2017 Diagnostic value of exome and whole genome sequencing in craniosynostosis.
PMID 29100083
2017 High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
PMID 15494731
2004 A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.