A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic Correlation
Badreddine Elmakhzen, Ayoub Nedbour, Laila Bouguenouch, Mohamed Ahakoud
0 citationsCureus
Ayoub Nedbour
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5Publications signalées
7Citations signalées
1Affiliations récentes
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Epilepsy research and treatmentDementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsEpigenetics and DNA MethylationIon channel regulation and function
Publications récentes
Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report
Hinde El Mouhi, Nada Amllal, Meriame Abbassi, Ayoub Nedbour et autres
1 citationMolecular Biology Reports
Identification of Novel and De Novo Mutation in the SCN1A Gene By Exome Sequencing Confirms Dravet Syndrome in Moroccan Child: A Case Report
Hinde El Mouhi, Nada Amllal, Meriame Abbassi, Ayoub Nedbour et autres
0 citationsResearch Square
Novel APOE Mutation in a Moroccan Subject Suffering from Alzheimer Disease
Youssef Razouqi, Ihssane El Bouchikhi, Hassan El‐Abid, Soukayna Baammi et autres
2 citationsAlzheimer Disease & Associated Disorders
The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study
Mohamed Ahakoud, Hanae Daha Belghiti, Ayoub Nedbour, Abdelhamid Bouramtane et autres
4 citationsCureus
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