mutation
153 results
1 - 100mutation
- 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
vemurafenib
gene
dabrafenib
escape
mutational escape
sport
trametinib
channelopathy
ivosidenib
revertant
enasidenib
dissociation
mitochondriopathy
idiovariation
mutein
cobimetinib
binimetinib
gilteritinib
deafness
encorafenib
lumacaftor/ivacaftor
enzymopathy
ivacaftor
eteplirsen
avapritinib
golodirsen
delta F-508
elexacaftor/tezacaftor/ivacaftor
transmutation
Bartlett-Biedel syndrome
diagnostic
phenocopy
factor
subtype
Denys-Drash syndrome
mosaic
transversion
dominant optic atrophy and deafness
panitumumab
midostaurin
genotype
osimertinib
viral breakthrough
larotrectinib
Ghent nosology
achondroplasia
Guillain-Barré Syndrome
rucaparib
tumor necrosis factor receptor-associated periodic syndrome
Hemophilia
Sickle Cell Disease
cetuximab
juvenile hemochromatosis
alpelisib
entrectinib
maternally inherited diabetes and deafness
Arterial Occlusive Disease
Goiter
Atrial Dysrhythmias
Duchenne, Guillaume B. A.
myelofibrosis
Sudden Infant Death Syndrome
Hypoglycemia
Hypophosphatemia
Leukemia, Chronic