Cite
HARVARD Citation
Litz Philipsborn, S. et al. (2021). A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. American journal of medical genetics. 185 (5), pp. 1610-1613. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Litz Philipsborn, S. et al. (2021). A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. American journal of medical genetics. 185 (5), pp. 1610-1613. [Online].