Your English writing platform
Discover LudwigSuggestions(1)
Exact(2)
MAX germline mutation is recently identified as a rare cause of hereditary PPGL.
Among the mtDNA mutations observed in these patients, the coding G8836C (ATP6) mutation is recently reported in patients with Leber Hereditary Optic Neuropathy (LHON -like syndrome and thyroid tumors [15]–[16].
Similar(58)
The V68 mutation was recently reported to be phylogenetically equivalent to M78 in a sample of 239 African chromosomes [4].
This mutation was recently reported in a patient that presented familial gastrointestinal stromal tumor and mastocytosis [21].
This mutation was recently reported in a large clinical database from a multi-center case-control study screening patients for LQT [40].
However a dominant mutation was recently found in this gene.
Ivacaftor, a corrector of the G551D mutation, was recently approved by the Food and Drug Administration.
Remarkably, a MYD88 L265P-activating mutation was recently found in 90% of WM cases.
This mutation was recently described in the LIG4 patient presenting with the Dubowitz syndrome [Yue et al., 2013].
The same mutation was recently identified in a compound heterozygous configuration with a A318T mutation in two siblings with a severe MDS (24).
Interestingly, the same mutation was recently found to be associated with melanism in another bird, the red-footed booby (Sula sula) [ 10].
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