Lack of evidence of ERVWE1/Xq22.3 involvement in MRSV transcripts detected in Multiple Sclerosis patients

Documenti analoghi

• HERV-W/MRSV envelope transcripts detection in blood of multiple sclerosis patients after Natalizumab treatment
  di: Nali, Luiz HS, et al.
  Pubblicazione: (2014)
• Genomic analysis of ERVWE2 locus in patients with multiple sclerosis: absence of genetic association but potential role of human endogenous retrovirus type W elements in molecular mimicry with myelin antigen
  di: do Olival, Guilherme S., et al.
  Pubblicazione: (2013)
• A male infant with Xq22.2q22.3 duplication containing PLP1 and MID2
  di: Chanchani, Swati R., et al.
  Pubblicazione: (2020)
• Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)
  di: Meloni, I, et al.
  Pubblicazione: (2002)
• Temporal skin folds in a female infant with an unbalanced translocation with breakpoints Xq22.1 and 6p22.3: a new association?
  di: Vasileiadis, G T, et al.
  Pubblicazione: (2013)