mutation
141 results
1 - 100
mutation- inactivating mutation
- conservative mutation
- induced mutation
- JAK2 mutation
- loss-of-function mutation
- missense mutation
- natural mutation
- nonconservative mutation
- nonsense mutation
- null mutation
- passenger mutation
- driver mutation
- point mutation
- regulatory mutation
- silent mutation
- somatic mutation
- targeted mutation
- transparent mutation
- engineered mutation
- escape mutation
- factor V Leiden mutation
- founder mutation
- frameshift mutation
- gain-of-function mutation
- germline mutation
- JAK2 mutation
- mutation frequency
- mutagenesis
- channelopathy
- gene
- sport
- escape
- mutational escape
- revertant
trametinib- dabrafenib
- dissociation
- deafness
- vemurafenib
- mitochondriopathy
- idiovariation
- mutein
- enasidenib
- delta F-508
- cobimetinib
- rucaparib
- transmutation
- enzymopathy
- Bartlett-Biedel syndrome
- phenocopy
- factor
- subtype
- diagnostic
- encorafenib
- transversion
- ivacaftor/lumacaftor
- Denys-Drash syndrome
- ivacaftor
- eteplirsen
- mosaic
- dominant optic atrophy and deafness
- viral breakthrough
- achondroplasia
- Ghent nosology
Guillain-Barré Syndrome- panitumumab
- genotype
- Sickle Cell Disease
- Hemophilia
- tumor necrosis factor receptor-associated periodic syndrome
- juvenile hemochromatosis
- midostaurin
- Goiter
- osimertinib
- cetuximab
- Duchenne, Guillaume B. A.
- maternally inherited diabetes and deafness
- Arterial Occlusive Disease
- myelofibrosis
- Atrial Dysrhythmias
- Leukemia, Chronic
- Hypoglycemia
- Sudden Infant Death Syndrome
- Gastric Cancer
- Hypercalcemia
- Hypophosphatemia
- polymorphism
- Fukuyama disease
- Ventricular Dysrhythmias
- McArdle disease
- Hypochloremia
- Amyotrophic Lateral Sclerosis