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GRACILE syndrome
Disease Reference Book
Neonatal Hemochromatosis: a Congenital Alloimmune Hepatitis
GRACILE Syndrome, a Lethal Metabolic Disorder with Iron
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Prenatal Comprehensive Requisition
SSIEM Classification of Inborn Errors of Metabolism 2011
Prenatal Testing Requisition
Mitokondriesykdommer
BCS1L Gene BCS1 Homolog, Ubiquinol-Cytochrome C Reductase Complex Chaperone
MOLECULAR GENETICS of the GRACILE SYNDROME (Growth Retardation, Aminoaciduria, Cholestasis, Iron Overload, Lactacidosis and Early Death)
33 Disorders of Copper, Zinc, and Iron Metabolism Eve A
Bruce H. Cohen, MD Page 1 of 56
Renal Manifestations of Primary Mitochondrial Disorders (Review)
Genetic Hearing Loss in Childhood and Oxygen Reactive Species
Leigh Syndrome and Mitochondrial Encephalopathy Precision Panel
Interventions to Improve Mitochondrial Function in a Mouse Model of GRACILE Syndrome, a Complex III Disorder
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Prenatal Testing Requisition
Top View
GRACILE Syndrome
GRACILE Syndrome/ BCS1L-Related Disorders
Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A
GRACILE Syndrome