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Title:          Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
Subject:        Neurobiology of Aging, 66 (2018) 181.e3-181.e10. doi:10.1016/j.neurobiolaging.2018.02.011
Author:         Stéphanie Philtjens
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      Title: Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
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        Title: 1. Introduction
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       Item: 
        Title: 2. Methods
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         Item: 
          Title: 2.1. Patient/control study populations
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         Item: 
          Title: 2.2. Ethical assurances
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         Item: 
          Title: 2.3. SORT1 sequencing
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         Item: 
          Title: 2.4. Haplotype sharing analysis
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         Item: 
          Title: 2.5. In silico predictions
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         Item: 
          Title: 2.6. Statistical analysis
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        Title: 3. Results
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         Item: 
          Title: 3.1. SORT1 variants in the Belgian cohorts
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          Title: 3.2. SORT1 variants in the European cohorts
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          Title: 3.3. Clinical characteristics of SORT1 patient-only variant carriers
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        Title: 4. Discussion
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        Title: Disclosure statement
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        Title: Acknowledgements
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        Title: Appendix A. Supplementary data
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        Title: References
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  Checksum: 1bde065f
   Type: CRC32
  Checksum: 0660fc6fc637fa03f72838d734be4d64
   Type: MD5
  Checksum: 1f1742c3f232ab13e6ae42fadb014513ce360da6
   Type: SHA-1
  Checksum: f921409bc77790b4f4dbb70cf09a850c3805832c5c1f983f8d37e44b8051512d
   Type: SHA-256