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Results: 5

Authors: KMOCH S ZEMAN J HREBICEK M RYBA L KRISTENSEN MJ GREGERSEN N
Citation: S. Kmoch et al., RIBOFLAVIN-RESPONSIVE EPILEPSY IN A PATIENT WITH SER209 VARIANT FORM OF SHORT-CHAIN ACYL-COA DEHYDROGENASE, Journal of inherited metabolic disease, 18(2), 1995, pp. 227-229

Authors: BROSS P JESPERSEN C JENSEN TG ANDRESEN BS KRISTENSEN MJ WINTER V NANDY A KRAUTLE F GHISLA S BOLUND L KIM JJP GREGERSEN N
Citation: P. Bross et al., EFFECTS OF 2 MUTATIONS DETECTED IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD)-DEFICIENT PATIENTS ON FOLDING, OLIGOMER ASSEMBLY, AND STABILITY OF MCAD ENZYME, The Journal of biological chemistry, 270(17), 1995, pp. 10284-10290

Authors: JENSEN HK HANSEN PS JENSEN LG KRISTENSEN MJ KLAUSEN IC KJELDSEN M LEMMING L BOLUND L GREGERSEN N FAERGEMAN O
Citation: Hk. Jensen et al., COMPLEXITY OF MOLECULAR-GENETICS OF DYSLIPIDEMIA IN A FAMILY HIGHLY SUSCEPTIBLE TO ISCHEMIC-HEART-DISEASE, Clinical genetics, 48(1), 1995, pp. 23-28

Authors: KRISTENSEN MJ KMOCH S BROSS P ANDRESEN BS GREGERSEN N
Citation: Mj. Kristensen et al., AMINO-ACID POLYMORPHISM (GLY209SER) IN THE ACADS GENE, Human molecular genetics, 3(9), 1994, pp. 1711-1711

Authors: KRISTENSEN MJ BHALA A HALE DE JENSEN TG GREGERSEN N
Citation: Mj. Kristensen et al., NEW POINT MUTATIONS IN SHORT-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY, American journal of human genetics, 53(3), 1993, pp. 915-915
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