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GFM1
Neuromuscular Disorders Neurology in Practice: Series Editors: Robert A
Supplementary Materials
Novel GFM2 Variants Associated with Early-Onset Neurological Presentations of Mitochondrial Disease and Impaired Expression of OXPHOS Subunits
Molecular Risk Factors of Pulmonary Arterial Hypertension Hamza M
Journal of Agric. 2011 Vol. 11 No. 1
Mitochondrial Medicine 2019: Washington DC 6FLHQWLÀFDQG&OLQLFDO0HHWLQJV June 26-29, 2019 Hilton Alexandria Mark Center Alexandria, VA
Compound Heterozygous GFM2 Mutations with Leigh Syndrome Complicated by Arthrogryposis Multiplex Congenita
UNIVERSITY of CALIFORNIA, IRVINE Whole Exome Sequencing
THE USE of WHOLE EXOME SEQUENCING to DETECT NOVEL GENETIC DISORDERS: TWO CASES and an ASSESSMENT of the TECHNOLOGY by Lauren
Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-Trna Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome
Genes and Variants Underlying Human Congenital Lactic Acidosis—From Genetics to Personalized Treatment
Wasin Vol. 9 N. 4 2558.Pmd
Novel GFM2 Variants Associated with Early-Onset Neurological Presentations of Mitochondrial Disease and Impaired Expression of OXPHOS Subunits
The Spider Woman Rules No More
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Platform Abstracts
GFM1 Gene G Elongation Factor Mitochondrial 1
Top View
Integrating Genomic Approaches to Understand Ageing Nomic Geing
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Download Sample Report
Hypermethylation of Human DNA: Fine-Tuning Transcription Associated with Development
UC Irvine UC Irvine Electronic Theses and Dissertations
Sixteen New Lung Function Signals Identified Through 1000 Genomes
Whole Body Vibration Training in Chronic Disease