Authors:
Athan, ES
Williamson, J
Ciappa, A
Santana, V
Romas, SN
Lee, JH
Rondon, H
Lantigua, RA
Medrano, M
Torres, M
Arawaka, S
Rogaeva, E
Song, YQ
Sato, C
Kawarai, T
Fafel, KC
Boss, MA
Seltzer, WK
Stern, Y
St George-Hyslop, P
Tycko, B
Mayeux, R
Citation: Es. Athan et al., A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families, J AM MED A, 286(18), 2001, pp. 2257-2263
Citation: Kj. Felice et Wk. Seltzer, Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G -> C), W44X(G -> A)] in the connexin 32 gene, EUR NEUROL, 44(1), 2000, pp. 61-63
Citation: Eb. Spector et al., Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization, MOL GEN MET, 67(4), 1999, pp. 364-367
Authors:
Holmes, SE
O'Hearn, EE
McInnis, MG
Gorelick-Feldman, DA
Kleiderlein, JJ
Callahan, C
Kwak, NG
Ingersoll-Ashworth, RG
Sherr, M
Sumner, AJ
Sharp, AH
Ananth, U
Seltzer, WK
Boss, MA
Vieria-Saecker, AM
Epplen, JT
Riess, O
Ross, CA
Margolis, RL
Citation: Se. Holmes et al., Expansion of a novel CAG trinucleotide repeat in the 5 ' region of PPP2R2Bis associated with SCA12, NAT GENET, 23(4), 1999, pp. 391-392