C. Z. Seco

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

H. Kremer, L. Hoefsloot, R. Pennings, 2014, European Journal of Human Genetics.

Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells

T. Strom, H. Kremer, S. Riazuddin, 2015, European Journal of Human Genetics.

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families

T. Strom, H. Kremer, A. Hussain, 2014, PloS one.

Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia

R. Holt, P. Calvas, N. Chassaing, 2019, Human Genetics.