cetylpyridinium chloride anhydrous and Autosomal Dominant Cerebellar Ataxia, Type II

cetylpyridinium chloride anhydrous has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Jiang, H; Liao, SS; Pan, Q; Shen, L; Tang, BS; Wang, JL; Xia, K; Xu, Q; Yan, XX; Zhang, S; Zhou, YF; Zhu, HX	1

Other Studies

1 other study(ies) available for cetylpyridinium chloride anhydrous and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han. Journal of genetics, 2008, Volume: 87, Issue:3 Topics: Adolescent; Adult; Alleles; Asian People; Ataxin-10; Base Sequence; Blotting, Southern; Case-Control Studies; Child; Child, Preschool; China; DNA Mutational Analysis; Genetic Variation; Health; Humans; Microsatellite Repeats; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Spinocerebellar Ataxias	2008

Article

Year

Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.

Journal of genetics, 2008, Volume: 87, Issue:3

Topics: Adolescent; Adult; Alleles; Asian People; Ataxin-10; Base Sequence; Blotting, Southern; Case-Control Studies; Child; Child, Preschool; China; DNA Mutational Analysis; Genetic Variation; Health; Humans; Microsatellite Repeats; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Spinocerebellar Ataxias

2008