Search Results - "Learning Disabilities complications"

PRRT2 mutations: exploring the phenotypical boundaries: exploring the phenotypical boundaries

Authors: Djemie, Tania Weckhuysen, S. Holmgren, Philippe et al.

Contributors: Djemie, Tania Weckhuysen, S. Holmgren, Philippe et al.

Source: Journal of neurology, neurosurgery and psychiatry

Subject Terms: Male, Epilepsy, Learning Disabilities, Motor Skills Disorders/complications, Membrane Proteins, Nerve Tissue Proteins, 7. Clean energy, Pedigree, Motor Skills Disorders, Learning Disabilities/complications, 03 medical and health sciences, Phenotype, 0302 clinical medicine, 13. Climate action, Nerve Tissue Proteins/genetics, Humans, Point Mutation, Female, Point Mutation/genetics, Human medicine, Membrane Proteins/genetics, Epilepsy/complications

Access URL: https://pubmed.ncbi.nlm.nih.gov/24101679
http://jnnp.bmj.com/content/85/4/462
https://researchportal.vub.be/en/publications/prrt2-mutations-exploring-the-phenotypical-boundaries
https://jnnp.bmj.com/content/jnnp/85/4/462.full.pdf
https://jnnp.bmj.com/content/85/4/462.full.pdf
https://www.ncbi.nlm.nih.gov/pubmed/24101679
https://jnnp.bmj.com/content/85/4/462
https://hdl.handle.net/10067/1172040151162165141
https://biblio.vub.ac.be/vubir/(1d061c24-3f0b-4d98-9871-4aa92b8bc248).html