Mutations in several other genes have been linked to noninherited forms of the disease.
Though H5 may seem only a couple of steps from transmissibility among people, many virologists believe mutations in several other genes would be necessary as well, even though those changes are not yet well understood.
Mutations in several sarcomere genes have been described in LVNC.
To date, mutations in several genes have been identified in patients with 46,XY DSD.
Genome sequencing identified acquired mutations in several human tumor suppressor homologs.
Mutations in several sarcomeric proteins have been linked to various human myopathies.
Mutations in several genes in Table 3 have been associated with diseases affecting cognitive capacities.
Effects of mutations in several charged residues within the Aβ linker region on aggregation have been extensively studied.
Recent studies have attributed non-syndromic tooth agenesis to mutations in several genes, including MSX1, PAX9, AXIN2, WNT10A and EDA.
Mutations in several Wnt members have been identified since then, including CTNNB1 [8] activating, APC [9] and Axin [10] inactivating, which account for 25%% of sporadic MB [11].
Mutations in several SWI/SNF subunits have been recently identified at a high frequency in a variety of cancers (Masliah-Planchon et al., 2015).
