A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report von Bouzroud, Wafaa, Tazzite, Amal, Boussakri, Ikhlass, Gazzaz, Bouchaïb, Dehbi, Hind

Volltext

R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report von Bouzroud, Wafaa, Tazzite, Amal, Berrada, Sarah, Gazzaz, Bouchaïb, Dehbi, Hind

Volltext

Complement Factor I deficiency: A novel homozygous CFI gene mutation von Bouzroud, Wafaa, Tazzite, Amal, yousra, Ibenbrahim, Gazzaz, Bouchaïb, Dehbi, Hind

Volltext

A novel variant of unknown significance in pediatric epilepsy: a case report von Wafaa Bouzroud, Amal Tazzite, Ikhlass Boussakri, Bouchaïb Gazzaz, Hind Dehbi

Volltext

Complement Factor I deficiency: A novel homozygous gene mutation von Wafaa Bouzroud, Amal Tazzite, Ibenbrahim yousra, Bouchaïb Gazzaz, Hind Dehbi

Volltext

Forme variante Angelman-like du syndrome de Rett confirmée par le séquençage haut débit d’exome : à propos d’un cas von Bouzroud, Wafaa, Berrada, Sarah, Hind, Dehbi

Volltext

Une déficience intellectuelle syndromique révélant une mutation en MAST1 von Bouzroud, Wafaa, Berrada, Sarah, Hind, Dehbi

Volltext

R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report von Wafaa Bouzroud, Amal Tazzite, Sarah Berrada, Bouchaïb Gazzaz, Hind Dehbi

Volltext

R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report von Bouzroud, Wafaa, Tazzite, Amal, Berrada, Sarah, Gazzaz, Bouchaïb, Dehbi, Hind

Volltext