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BioWorld Science, Biomarkers
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Researchers identify novel mutation in GBE1 gene in a GSD-IV patient

Sep. 17, 2015

QRLS1 mutations identified as a cause of infantile mitochondrial disease

Sep. 17, 2015

ALCAM mediates late kidney complications of diabetes

Sep. 16, 2015

STAT2 regulates mitochondrial fission

Sep. 16, 2015

LIPT2 gene mutations may be associated with lipoic acid biosynthesis defects

Sep. 15, 2015

Riboflavin metabolism abnormalities may induce MADD

Sep. 15, 2015

Elevated N-acetylspermidine, a potential biomarker for Snyder Robinson syndrome

Sep. 15, 2015

Novel PI4K2A gene mutations identified in cutis laxa syndrome with choreoathetosis

Sep. 14, 2015

Relaxin levels linked to risk of death in patients with acute heart failure

Sep. 9, 2015

Mitochondrial DNA mutation linked to mitochondrial hepatopathy

Sep. 9, 2015

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