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Faisal Fecto
Stanford University - Stanford / United States
Medical and Health Sciences / Neuroscience
AD Scientific Index ID: 1651314
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Faisal Fecto's MOST POPULAR ARTICLES
1-)
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaHX Deng, W Chen, ST Hong, KM Boycott, GH Gorrie, N Siddique, Y Yang, ...Nature 477 (7363), 211-215, 201112612011
2-)
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosisF Fecto, J Yan, SP Vemula, E Liu, Y Yang, W Chen, JG Zheng, Y Shi, ...Archives of neurology 68 (11), 1440-1446, 20116772011
3-)
FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosisHX Deng, H Zhai, EH Bigio, J Yan, F Fecto, K Ajroud, M Mishra, ...Annals of neurology 67 (6), 739-748, 20103902010
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Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4HX Deng, CJ Klein, J Yan, Y Shi, Y Wu, F Fecto, HJ Yau, Y Yang, H Zhai, ...Nature genetics 42 (2), 165-169, 20103052010
5-)
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, HX Deng, N Siddique, F Fecto, W Chen, Y Yang, E Liu, ...Neurology 75 (9), 807-814, 20102432010
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