Ntrk2 (neurotrophic tyrosine kinase, receptor, type 2)

基因基本信息

Ntrk2 基因表型（MGI）

Different lines of homozygous mice show varied abnormalities including innervation and neural defects, rod defects, impaired ovarian folliculogenesis, and reduced postnatal survival. Homozygotes for a point mutation are normal, but are subject to pharmacological control of signalling.

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