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Yi Chuan Xue Bao = Acta Genetica Sinica|February 9, 2000
[Molecular cloning of one splicing form of human M6b cDNA]J H Xia, C Y Liu, Q G Ruan, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Nature|March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.
Science (New York, N.Y.)|August 20, 1993
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutaseH X Deng, A Hentati, J A Tainer, et al.
Neurogenetics|May 1, 1997
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosisJ S Zu, H X Deng, T P Lo, et al.
Human Molecular Genetics|September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
Science (New York, N.Y.)|June 17, 1994
Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutationM E Gurney, H Pu, A Y Chiu, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|July 2, 1998
[Localization of the gene for 4 hereditary multiple exostoses families]Y Tang, J H Xia, J N Zhou, et al.
Neurology|August 9, 2006
Lack of association of VEGF promoter polymorphisms with sporadic ALSW Chen, M Saeed, H Mao, et al.
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