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Costeff syndrome
Peripheral Neuropathy in Complex Inherited Diseases: an Approach To
Genes in Eyecare Geneseyedoc 3 W.M
Dominant Optic Atrophy
Optic Atrophy, Cataracts, Lipodystrophy/Lipoatrophy and Peripheral Neuropathy Caused by a De Novo OPA3 Mutation
A Model of Costeff Syndrome Reveals Metabolic and Protective Functions of Mitochondrial OPA3 Wuhong Pei1, Lisa E
Defects in Amino Acid Catabolism and the Urea Cycle
Costeff Syndrome
Two Novel Compound Heterozygous Mutations in OPA3 in Two Siblings with OPA3-Related 3-Methylglutaconic Aciduria
A Missense Mutation in the Murine Opa3 Gene Models Human Costeff
Movement Disorders and Neurometabolic Diseases
Metabolic Stroke in a Patient with Bi-Allelic OPA1 Mutations
Optic Atrophy, Cataracts, Lipodystrophy/Lipoatrophy, and Peripheral Neuropathy Caused by a De Novo OPA3 Mutation
1 a Clinical Approach to Inherited Metabolic Diseases
Behr's Syndrome Is Typically Associated with Disturbed
3-Methylglutaconic Aciduria Type III in a Non-Iraqi-Jewish Kindred: Clinical and Molecular findings
3-Methylglutaconic Aciduria
Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies
OPA3 Gene OPA3, Outer Mitochondrial Membrane Lipid Metabolism Regulator
Top View
Using Electrophysiology to Explore Retinal Function in Autosomal Dominant Optic Atrophy
Mendelian Disorders Among Jews