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Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy
Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy
2017
R. Van Coster
Hedwig Stepman
Arnaud Vanlander
Joél Smet
Sara Seneca
Elise Vantroys
L. De Meirleir
Keywords:
Physical therapy
Endocrinology
Diabetes mellitus
Riboflavin
Familial Hypertrophic Cardiomyopathy
Internal medicine
Medicine
Locus heterogeneity
Mutation
Correction
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