Molecular analysis of the arylsulphatase A gene in late infantile metachromatic leucodystrophy patients and healthy subjects from Italy.

Author:

Regis S,Filocamo M,Stroppiano M,Corsolini F,Gatti R

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. Metachromatic leukodystrophy and multiple sulfatase deficiency: sulfatide lipidosis;Kolodny, E.H.; Fluharty, A.L.,1994

2. Molecular genetics of metachromatic leukodystrophy;Gieselmann, V.; Zlotogora, J.; Harris, A.; Wenger, D.A.; Morris, C.P.;Hum Mutat,1994

3. Simultaneous detection of the two most frequent metachromatic leukodystrophy mutations;Berger, J.; Molzer, B.; Gieselmann, V.; Bemheimer, H.;Hum Genet,1993

4. An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromic leukodystrophy;Gieselmann, V.;Hum Genet,1991

5. The assay of arylsulfatase A and B in human urine;Baum, H.; Dogson, K.S.; Spencer, B.;Clin Chim Acta,1959

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