Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

Những quyển sách tương tự

• A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family()
  Bằng: Guerreiro, Rita, et al.
  Được phát hành: (2013)
• Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia
  Bằng: Guven, Gamze, et al.
  Được phát hành: (2019)
• Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
  Bằng: Guven, Gamze, et al.
  Được phát hành: (2016)
• Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.
  Bằng: Gamze Guven, et al.
  Được phát hành: (2016-01-01)
• Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
  Bằng: Guerreiro, Rita Joao, et al.
  Được phát hành: (2011)