mirror movements 4

Term ID

DOID:0070638

Synonyms

Definition

A congenital mirror movement disorder that has_material_basis_in heterozygous mutation in the NTN1 gene on chromosome 17p13. https://pmc.ncbi.nlm.nih.gov/articles/PMC5663368/

References

• MIM:618264

Ontology

Human Disease   ( DOID:0070638 )