María Lachgar-Ruiz

3PUBLICATIONS
15CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionGene mapping
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Publications (3)

|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants.

María Lachgar-Ruiz, Matías Morín, Elisa Martelletti

|Jun 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.

Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar

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