Biochemistry, Genetics and Molecular Biology
Gene
100%
Genetics
41%
Missense
35%
Spectrum
31%
Mitochondrial RNA
31%
Frameshift Mutation
31%
Adenylosuccinate Lyase
31%
Liquid
20%
Molecular Genetics
20%
Transversion
15%
DNA Mutation
10%
Transcription
10%
Mitochondrial Disorder
10%
Gene Product
10%
Ribonuclease
10%
Proband
10%
RNA
10%
Enzyme
10%
Genome Sequencing
10%
Purine Metabolism
10%
Genetic Prenatal Diagnosis
10%
Autosomal Recessive Disorder
10%
Anabolism
5%
Magnetism
5%
Spectroscopy
5%
Medicine and Dentistry
Patient
65%
Disease
34%
Child
31%
Syndrome
31%
Liver Transplantation
31%
DNA Mutation
31%
Mitochondrial DNA
31%
Mitochondrial DNA Disorder
15%
Cytochrome C Oxidase Deficiency
15%
Sensorineural Hearing Loss
15%
Lactic Acidosis
15%
Gene
15%
Point Mutation
15%
Brain Disease
15%
Chronic Progressive External Ophthalmoplegia
15%
Cerebrospinal Fluid
12%
Age
9%
Quality of Life
9%
Epilepsy
6%
Blood Glucose
6%