NDPT095
96 WELL PLATE OF DNA SAMPLES
Description:
NEUROLOGICALLY NORMAL WHITE CONTROL PANEL
Aliquot Size:
5 µg each
Sex:
Males: 46 Females: 48
Brief Description:
This panel contains 5 micrograms of DNA from 94 unique and unrelated White non-Hispanic individuals from North America without neurological disorders. Of these, 46 are males and 48 are females, with an age at collection ranging from 58 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. As an internal control, ND09230 appears twice on the panel, in F08 and well H12. Well C02 is empty for addition of a laboratory control.
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 |
| |
| Jenkinson EM, Rodero MP, Kasher PR, Uggenti C, Oojageer A, Goosey LC, Rose Y, Kershaw CJ, Urquhart JE, Williams SG, Bhaskar SS, O'Sullivan J, Baerlocher GM, Haubitz M, Aubert G, Barañano KW, Barnicoat AJ, Battini R, Berger A, Blair EM, Brunstrom-Hernandez JE, Buckard JA, Cassiman DM, Caumes R, Cordelli DM, De Waele LM, Fay AJ, Ferreira P, Fletcher NA, Fryer AE, Goel H, Hemingway CA, Henneke M, Hughes I, Jefferson RJ, Kumar R, Lagae L, Landrieu PG, Lourenço CM, Malpas TJ, Mehta SG, Metz I, Naidu S, Õunap K, Panzer A, Prabhakar P, Quaghebeur G, Schiffmann R, Sherr EH, Sinnathuray KR, Soh C, Stewart HS, Stone J, Van Esch H, Van Mol CE, Vanderver A, Wakeling EL, Whitney A, Pavitt GD, Griffiths-Jones S, Rice GI, Revy P, van der Knaap MS, Livingston JH, O'Keefe RT, Crow YJ, Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts Nature genetics48:1185-92 2015 |
| PubMed ID: 27571260 |
| |
| 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 pain48:1185-92 2015 |
| PubMed ID: 25585270 |
| |
| 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 |
|
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