Cite
MLA Citation
Shira Litz Philipsborn et al.. “A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.” American journal of medical genetics, vol. 185, no. 5, 2021, pp. 1610–1613. http://access.bl.uk/ark:/81055/vdc_100127439205.0x00001a