A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. Issue 5 (15th February 2021) - Litz Philipsborn, Shira; Hartmajer, Shulamit; Shtorch Asor, Atalia; Vinovezky, Mika; Regev, Miriam; Singer, Amihood; Reinstein, Eyal