MCAD deficiency in Denmark-Reference-Cited by-同舟云学术

MCAD deficiency in Denmark

Published:2012-06 Issue:2 Volume:106 Page:175-188
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Andresen Brage Storstein,Lund Allan Meldgaard,Hougaard David Michael,Christensen Ernst,Gahrn Birthe,Christensen Mette,Bross Peter,Vested Anne,Simonsen Henrik,Skogstrand Kristin,Olpin Simon,Brandt Niels Jacob,Skovby Flemming,Nørgaard-Pedersen Bent,Gregersen Niels

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference57 articles.

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2. Mitochondrial fatty acid oxidation defects — remaining challenges;Gregersen;J. Inherit. Metab. Dis.,2008

3. Fatty-acid oxidation defects;Strauss,2009

4. Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency*

5. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program;Zytkovicz;Clin. Chem.,2001

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