Author

Afaf Benitto

Observed institutions: Centre Hospitalier Universitaire de Reims, Centre Hospitalier Universitaire Ibn Rochd

OpenAlex ID: A5050771489

Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go

2021 · Tamara Dangouloff, Eva Vrščaj, et al. · Neuromuscular Disorders · 186

A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN 2A and PRRT 2

2013 · Sarra Dimassi, Audrey Labalme, et al. · Epilepsia · 76

Duchenne muscular dystrophy: Advances in molecular appraoch

2013 · Afaf Benitto, Khalil Hamzi, et al. · Indian journal of human genetics

Works count: 3

Citation count: 262

H-index: 2

I10-index: 2