A TaqI RFLP for the human arylsulfatase A gene
- PMID: 1979166
- PMCID: PMC332686
- DOI: 10.1093/nar/18.22.6746-a
A TaqI RFLP for the human arylsulfatase A gene
Similar articles
-
A BamHI RFLP in the human arylsulfatase A gene.Nucleic Acids Res. 1990 Nov 25;18(22):6746. doi: 10.1093/nar/18.22.6746. Nucleic Acids Res. 1990. PMID: 1979165 Free PMC article.
-
Novel mutations in arylsulfatase A gene in three Ukrainian families with metachromatic leukodystrophy.Mol Genet Metab. 2003 Nov;80(3):360-3. doi: 10.1016/j.ymgme.2003.08.004. Mol Genet Metab. 2003. PMID: 14680985
-
Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotype.Am J Med Genet. 1994 Aug 15;52(2):146-50. doi: 10.1002/ajmg.1320520205. Am J Med Genet. 1994. PMID: 7801999
-
Rapid detection of common mutation of arylsulfatase A in metachromatic leukodystrophy by polymerase chain reaction with a mismatched primer.J Child Neurol. 1994 Jan;9(1):38-40. doi: 10.1177/088307389400900108. J Child Neurol. 1994. PMID: 7908679
-
[Deficiency of arylsulfatase A activity as a basis of metachromatic leucodystrophy].Postepy Biochem. 1996;42(3):284-9. Postepy Biochem. 1996. PMID: 9036380 Review. Polish. No abstract available.
Cited by
-
Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3.Am J Hum Genet. 1994 Mar;54(3):464-72. Am J Hum Genet. 1994. PMID: 7906921 Free PMC article.
-
Search for putative suppressor genes in meningioma: significance of chromosome 22.Hum Genet. 1992 Mar;88(5):579-82. doi: 10.1007/BF00219348. Hum Genet. 1992. PMID: 1551661
-
Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation.Am J Hum Genet. 1997 Jan;60(1):113-20. Am J Hum Genet. 1997. PMID: 8981954 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources