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Scientists develop gene therapy approach for rare paralyzing disease

The 50 families stretch from the Netherlands and the United Kingdom to the United States and China. Each family has a child who is paralyzed from a mutation in a single gene named Contactin-Associated Protein 1 (Cntnap1).

United statesCheng changQian shiUnited kingdomDanielle ellisLong school of medicineJohn doran family foundation for neuropathyNational instituteUs national institutes of healthDepartment of cellularZachry foundationTeresa lozano long school of medicineUt health science center san antonioContactin associated proteinSouth texasManzoor bhat

Team looking at gene therapy for children paralyzed by rare mutations

Team looking at gene therapy for children paralyzed by rare mutations
medicalxpress.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from medicalxpress.com Daily Mail and Mail on Sunday newspapers.

United statesUnited kingdomCheng changQian shiUt health science center san antonioDepartment of cellularTeresa lozano long school of medicineLong school of medicineZachry foundationCell reportsContactin associated proteinSouth texasManzoor bhatTexas health science centerSan antonioLacey sell

Team Explores Gene Therapy for Paralysis in Children

Team Explores Gene Therapy for Paralysis in Children
miragenews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from miragenews.com Daily Mail and Mail on Sunday newspapers.

Cheng changUnited statesUnited kingdomQian shiUs national institutes of healthUt health science center san antonioZachry foundationNational instituteJohn doran family foundation for neuropathyUs department of educationLong school of medicineTeresa lozano long school of medicineDepartment of cellularContactin associated proteinSouth texasManzoor bhat