Shulamit Hartmajer

1PUBLICATIONS
0CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (1)

|Feb 16, 2021
A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.

Shira Litz Philipsborn, Shulamit Hartmajer, Atalia Shtorch Asor

Pageof 1

Frequent Collaborators