Tina Likar

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss

B. Peterlin, A. Maver, N. Teran, 2018, PloS one.