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Publications by Kaouther Ajroud

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Molecular Neuroscience

English

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A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy

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a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family

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A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

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Two Novel Mutations in the SLC25A4 Gene in a Patient With Mitochondrial Myopathy

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Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family

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Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes

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A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

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Death-Associated Protein 3 Regulates Mitochondrial-Encoded Protein Synthesis and Mitochondrial Dynamics

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Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene

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