Your English writing platform
Discover LudwigExact(4)
These mutations account only for a minority of cases, and much remains to be learnt about the molecular architecture of febrile seizures.
As K650M and K650E mutations account only for a minority of the FGFR3-related dysplasia cases (4.9%) [1], activation of STAT1 does not cause the disease in majority of the cases (Fig. 4).
FZD6 mutations account only for 1% of the NTDs cases.
While several predisposing genetic mutations have been found, these individual mutations account only for a small fraction of cancer incidence and mortality.
Similar(56)
Genetic factors also have an impact on risk, although the most common mutations account for only 2 3% of breast cancers.
However, CDH1 mutations account for only 1%3%% of all GCs.
KRAS mutations account for only 30%40%% of non-responders to EGFR targeting in colorectal cancer.
However, BRCA1/2 mutations account for only a small subgroup of women with a family history of breast cancer.
Together these mutations account for only a small proportion (2% to 5%) of all breast cancer incidences [ 2, 3].
However, these mutations account for only half of the cases that have been studied, which indicates that mutations in other genes may also cause Joubert syndrome.
At present, however, those mutations account for only a portion of familial cases, and consequently there is an intensive search for additional targets.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com