Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration

Author:

Wauters Eline,Gossye Helena,Frydas Alexandros,Sieben Anne,Van Broeckhoven ChristineORCID

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference45 articles.

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2. Promoter DNA methylation regulates progranulin expression and is altered in frontotemporal lobar degeneration (FTLD);Banzhaf-Strathmann;Acta Neuropathol. Commun.,2013

3. Staging of Alzheimer's disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry;Braak;Acta Neuropathol.,2006

4. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family;Brouwers,2007

5. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21;Cruts;Nature,2006

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