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M A M van den Brand

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Clinical Genetics|July 4, 2017
NDUFA9 point mutations cause a variable mitochondrial complex I assembly defectF Baertling, L Sánchez-Caballero, M A M van den Brand, et al.
Journal of Medical Genetics|October 24, 2007
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyA I Jonckheere, M Hogeveen, L G J Nijtmans, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
Clinical Genetics|July 4, 2017
NDUFA9 point mutations cause a variable mitochondrial complex I assembly defectF Baertling, L Sánchez-Caballero, M A M van den Brand, et al.
Journal of Medical Genetics|October 24, 2007
A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyA I Jonckheere, M Hogeveen, L G J Nijtmans, et al.
Pageof 1