Your English writing platform
Discover LudwigSuggestions(1)
Exact(1)
Likewise, great molecular heterogeneity in VLCADD [8] makes extended mutation screening obligatory in most cases.
Similar(59)
Jaijo, T. et al. MYO7A mutation screening in Usher syndrome type I patients from diverse origins.
Barandika, O. et al. A Cost-Effective Mutation Screening Strategy for Inherited Retinal Dystrophies.
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
Mutation screening was performed for known FHM-related genes.
In cases of SDHB mutation screening as early as 10 years of age is recommended.
Mutation screening of COL5A2 was normal.
GrP performed mutation screening.
Mutation screening was performed.
CM did KRAS mutation screening.
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