A. Paprotta

发表

Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene

K. Gerbitz, S. Zierz, M. Jaksch, 1993, FEBS letters.

Human Nesidioblastosis Tissue as an Immunogen for Generation of Islet Cell Specific Monoclonal Antibodies

K. Gerbitz, G. Hübner, A. Paprotta, 1988, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie.

Monoclonal antibodies against human islets of Langerhans

K. Gerbitz, A. Paprotta, B. Boenke, 1988 .

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.

K. Gerbitz, S. Hofmann, M. Jaksch, 1997, Human molecular genetics.

No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON

K. Gerbitz, K. Zerres, B. Obermaier-Kusser, 1992, FEBS letters.

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

T. Meitinger, B. Lorenz, K. Zerres, 1994, American journal of human genetics.