D. Zengeler

Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3.

T. Acker, B. Garvalov, C. Jux, 2018, Molecular genetics and metabolism.

Proteomic and morphological insights and clinical presentation of two young patients with novel mutations of BVES (POPDC1).

C. Depienne, A. Sickmann, P. F. van der Ven, 2022, Molecular genetics and metabolism.

Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome

J. Weis, J. Schulz, S. Biskup, 2022, Neurological Research and Practice.

The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy"

T. Acker, J. Schuld, P. F. van der Ven, 2021, Journal of Muscle Research and Cell Motility.

The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy"

T. Acker, J. Schuld, U. Ahting, 2021, Journal of Muscle Research and Cell Motility.

Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers

K. Claeys, J. Weis, J. Schulz, 2022, Neurological Research and Practice.

Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3.

T. Acker, B. Garvalov, C. Jux, 2018, Molecular genetics and metabolism.