Karin Roesch

DMEK Failure Associated with Innate Immune Activation

M. Zumbansen, S. Oellerich, G. Melles, 2019 .

The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex.

L. Tranebjaerg, C. Koehler, R. Varga, 2004, Human molecular genetics.

Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex.

L. Tranebjaerg, C. Koehler, S. Curran, 2002, Human molecular genetics.

Contiguous X-chromosome Deletion Syndrome Encompassing the BTK, TIMM8A, TAF7L, and DRP2 Genes

H. Ochs, K. Sullivan, A. Šedivá, 2007, Journal of Clinical Immunology.