Hinde El Mouhi

2PUBLICATIONS
0CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (2)

|Sep 26, 2025
Whole Exome Sequencing Identifies Novel Homozygous LGI1 Variant Mimicking ADAM22-Related Pathologies in a Moroccan Family.

Hinde El Mouhi, Badreddine Elmakhzen, Amina Bouyahyaoui

|Jan 28, 2024
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

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