NDPT098
96 WELL PLATE OF DNA SAMPLES
Description:
NEUROLOGICALLY NORMAL WHITE CONTROL PANEL
Aliquot Size:
5 µg each
Sex:
Males: 46 Females: 46
Brief Description:
This panel contains 5 micrograms of DNA from 92 unique and unrelated White individuals from North America without neurological disorders. Of these, 46 are males and 46 are females, with age at collection ranging from 56 through =>90 years. Data collected on these subjects consisted of Control Clinical Data Elements as outlined in the Coriell NINDS Genetics Repository guidelines. These data include a detailed medical and family history. None have a history of neurological illness in themselves, nor a first degree relative with a known primary neurological disorder. A more detailed description is also available. NDPT098 replaces NDPT022 and has the same samples except ND01697, ND07103, and ND01575 have been removed (no longer available) and replaced with ND10743, ND11515, and ND12254.
Plate Layout:
The specific position on the plates has been randomized to reduce
any possibility of systematic errors during the genotyping process.
| Estrada K, Whelan CW, Zhao F, Bronson P, Handsaker RE, Sun C, Carulli JP, Harris T, Ransohoff RM, McCarroll SA, Day-Williams AG, Greenberg BM, MacArthur DG, A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica Nature communications9:1929 2018 |
| PubMed ID: 29769526 |
| |
| Li QS, Cheng P, Favis R, Wickenden A, Romano G, Wang H, SCN9A Variants may be Implicated in Neuropathic Pain Associated with Diabetic Peripheral Neuropathy and Pain Severity The Clinical journal of pain9:1929 2015 |
| PubMed ID: 25585270 |
| |
| Ferrari R, Mok K, Moreno JH, Cosentino S, Goldman J, Pietrini P, Mayeux R, Tierney MC, Kapogiannis D, Jicha GA, Murrell JR, Ghetti B, Wassermann EM, Grafman J, Hardy J, Huey ED, Momeni P, Screening for C9ORF72 repeat expansion in FTLD Neurobiology of aging33:1850.e1-11 2012 |
| PubMed ID: 22459598 |
| |
| Ferrari R, Moreno JH, Minhajuddin AT, O'Bryant SE, Reisch JS, Barber RC, Momeni P, Implication of common and disease specific variants in CLU, CR1, and PICALM Neurobiology of aging33:1846.e7-18 2011 |
| PubMed ID: 22402018 |
| |
| Huey ED, Ferrari R, Moreno JH, Jensen C, Morris CM, Potocnik F, Kalaria RN, Tierney M, Wassermann EM, Hardy J, Grafman J, Momeni P, FUS and TDP43 genetic variability in FTD and CBS Neurobiology of aging33:1016.e9-17 2011 |
| PubMed ID: 21943958 |
| |
| Lee T, Li YR, Chesi A, Hart MP, Ramos D, Jethava N, Hosangadi D, Epstein J, Hodges B, Bonini NM, Gitler AD, Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis Neurology76:2062-5 2011 |
| PubMed ID: 21562248 |
|