Johannes Koch

发表

Deficiency of mitochondrial ATP synthase of nuclear genetic origin

E. Holme, J. Zeman, J. Houštěk, 2006, Neuromuscular Disorders.

Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: data from the E-HOD registry

M. Baumgartner, B. Seifert, H. Blom, 2018, Journal of Inherited Metabolic Disease.