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A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.
A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.
2021
Shira Litz-Philipsborn
Shulamit Hartmajer
Atalia Shtorch-Asor
Mika Vinovezky
Miriam Regev
Amihood Singer
Eyal Reinstein
Keywords:
Founder mutation
Genealogy
Meckel-Gruber Syndrome
Biology
Correction
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