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Items: 5

1.
First Record Mutations in the Genes ASPA and ARSA Causing Leukodystrophy in Jordan
Tawfiq Froukh
Biomed Res Int. 2019; 2019: 7235914. Published online 2019 Jan 30. doi: 10.1155/2019/7235914
PMCID:
PMC6374869
AbstractArticlePDF–1.2M
2.
Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.
K Narahara, Y Takahashi, M Murakami, K Tsuji, Y Yokoyama, R Murakami, S Ninomiya, Y Seino
J Med Genet. 1992 Jun; 29(6): 432–433. doi: 10.1136/jmg.29.6.432
PMCID:
PMC1016000
SummaryPage BrowsePDF–432K
3.
Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and B
Chester DeLuca, Judith A. Brown, Thomas B. Shows
Proc Natl Acad Sci U S A. 1979 Apr; 76(4): 1957–1961. doi: 10.1073/pnas.76.4.1957
PMCID:
PMC383512
SummaryPage BrowsePDF–1.2M
4.
Circular RNA expression profile and potential function of hsa_circ_0045272 in systemic lupus erythematosus
Lian‐Ju Li, Zhi‐Wei Zhu, Wei Zhao, Sha‐Sha Tao, Bao‐Zhu Li, Shu‐Zhen Xu, Jie‐Bing Wang, Ming‐Yue Zhang, Jun Wu, Rui‐Xue Leng, Yin‐Guang Fan, Hai‐Feng Pan, Dong‐Qing Ye
Immunology. 2018 Sep; 155(1): 137–149. Published online 2018 May 23. doi: 10.1111/imm.12940
PMCID:
PMC6099170
AbstractArticlePDF–1.3M
5.
The use of targeted genomic capture and massively parallel sequencing in diagnosis of Chinese Leukoencephalopathies
Xiaole Wang, Fang He, Fei Yin, Chao Chen, Liwen Wu, Lifen Yang, Jing Peng
Sci Rep. 2016; 6: 35936. Published online 2016 Oct 25. doi: 10.1038/srep35936
PMCID:
PMC5078786
AbstractArticlePDF–661K

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