Lina Basel-Salmon

6PUBLICATIONS
26CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Sep 30, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder.

Asier Iturrate, Nurit Assia Batzir, Ranit Jaron

|Apr 17, 2024
Exploring inheritance, and clinical penetrance of distal Xq28 duplication syndrome: insights from 47 new unpublished cases.

Michal Levy, Eyal Elron, Mordechai Shohat

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Frequent Collaborators

2 joint publications

Ashley Pritchard

2 joint publications

Rotem Greenberg

2 joint publications

Paula Jorge

2 joint publications

Francesca Romana Grati