Avidan, Nili

A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel

Lahat, H., Pras, E., Olender, T., Avidan, N., Ben-Asher, E., Man, O., Levy-Nissenbaum, E., Khoury, A., Lorber, A., Goldman, B., et al. (2001) · The American Journal of Human Genetics

Cardiac electrophysiology and arrhythmiasIon channel regulation and function

Cited by 655

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

Dgany, O., Avidan, N., Delaunay, J., Krasnov, T., Shalmon, L., Shalev, H., Eidelitz-Markus, T., Kapelushnik, J., Cattan, D., Pariente, A., et al. (2002) · The American Journal of Human Genetics

Hemoglobinopathies and Related DisordersErythrocyte Function and Pathophysiology

Cited by 168

Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy

Nakabayashi, K., Amann, D., Ren, Y., Saarialho-Kere, U., Avidan, N., Gentles, S., MacDonald, J. R., Puffenberger, E. G., Christiano, A. M., Martinez-Mir, A., et al. (2005) · The American Journal of Human Genetics

Hair Growth and DisordersSkin and Cellular Biology Research

Cited by 90