The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?
Brage Storstein Andresen(University of Southern Denmark), Niels Gregersen(Aarhus University), Daniel E. Hale(The University of Texas at San Antonio Health Science Center), Glenda Gray(South African Medical Research Council), Seymour Packman(University of California, San Francisco), Vibeke Winter(Aarhus University), Inga Knudsen(Aarhus University), Szabolcs Udvari(University College Dublin), Ichiro Yokota(Yale University), Steen Kølvraa(Aarhus University), Stanislav Kmoch(Charles University), Peter Bross(Aarhus University), K Hart(University of California, San Francisco), N. Chamoles(Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia), J P Harpey(Sorbonne Université), Jean Marie Saudubray(Université Paris Cité), J M Kirk(Royal Hospital for Children), Lars Bolund(BGI Group (China)), Bridget Wilcken(The University of Sydney)
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