Your English writing platform
Discover LudwigSuggestions(5)
Exact(8)
Thus, somatic mutations are increasingly seen as epiphenomena and subsequent events [14, 15].
However, FHM2 mutations are increasingly being recognised to be associated with cerebellar problems [24], childhood convulsions (benign familial infantile convulsions) [25], epilepsy [20, 26], alternating hemiplegia of childhood [27], and permanent mental retardation [20, 28].
Mitochondrial DNA (mtDNA) mutations are increasingly becoming recognised as important causes of disease.
Accidental carrier mutations are increasingly being reported as the use of multigenic screening with MPS increases [ 23, 27].
Post-zygotic, somatic mosaic mutations are increasingly recognized as an important cause of disease across a range of disorders.
NR5A1 loss-of-function mutations are increasingly found to be the cause of 46,XY disorders of sex development (DSD).
Similar(52)
Analysis for both mutations is increasingly being performed on patients exhibiting hypercoagulability.
The identification of somatically acquired tumor mutations is increasingly important in the clinical management of cancer because the sensitivity of targeted drugs is related to the genetic makeup of individual tumors.
Numerous mutations in crystallins have been identified to cause autosomal dominant congenital cataracts (ADCCs) and the list of mutations is increasingly risen every year (Shiels and Hejtmancik, 2015).
12– 14 Thus, molecular diagnosis of these mutations is increasingly important in making therapeutic decisions.
Molecular profiling to identify targetable driver mutations is increasingly being applied in the clinic, and can stratify patient groups.
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