H H Dahl

Leigh syndrome: Clinical features and biochemical and DNA abnormalities

S. Rahman, Rozanne B. Blok, H H Dahl et al. · Annals of Neurology · 1996 · 776 citations

Down Syndrome, Complex Iv-deficient Sibships, Genetic Testing +13

The construction of cosmid libraries which can be used to transform eukaryotic cells

F Grosveld, Torben Lund, Edward J. Murray et al. · Nucleic Acids Research · 1982 · 316 citations · Full text

Engineering, Reverse Genetics, Genetics +28

Respiratory chain complex I deficiency

Denise M. Kirby, Megan Crawford, Maureen Cleary et al. · Neurology · 1999 · 264 citations

The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA.

H H Dahl, S. M. Hunt, Wendy Hutchison et al. · Journal of Biological Chemistry · 1987 · 142 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +17

Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

Katherine R. Smith, H H Dahl, Laura Canafoglia et al. · Human Molecular Genetics · 2013 · 127 citations · Full text

Genetics, Kufs Disease, Pathology +16