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Items: 3

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

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