Devorah Yefet

Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss

D. Corey, J. Ekstein, K. Booth, 2021, Frontiers in Genetics.

Opposing effects of intracellular versus extracellular adenine nucleotides on autophagy: implications for β-cell function

B. Tirosh, Ann Saada, E. Cerasi, 2018, Journal of Cell Science.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.