Lior Tolkin

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 2

Top Topics

Amyotrophic Lateral Sclerosis

Top Venues

Journal of the Endocrine Society

This page only lists publications with an associated author ORCID identifier.

Publications

Lior Tolkin, Vanessa Klein, Meir Frankel, Gheona Altarescu, Rachel Beeri, Gabriel Munter
Variant Tyr 394Ser in the GCM2 Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism. Journal of the Endocrine Society 7 (7) (2023)
Lior Tolkin, Vanessa Klein, Meir Frankel, Gheona Altarescu, Rachel Beeri, Gabriel Munter
Variant Tyr 394Ser in the GCM2 Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism. Journal of the Endocrine Society 7 (7) (2023)