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Publications by Nailah Siddique

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

Molecular Neuroscience

English

Association of a Structural Variant Within the SQSTM1 Gene With Amyotrophic Lateral Sclerosis

Neurology: Genetics

English

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A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy

Journal of Medical Genetics

English

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

G3: Genes, Genomes, Genetics

Molecular Biology

English

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

American Journal of Human Genetics

English

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

Internal Medicine

Molecular Biology

English

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

Bioscience Reports

Molecular Biology

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

Internal Medicine

English

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

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

Journal of Biological Chemistry

Molecular Biology

English

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

Archives of Neurology

English