The arylsulphatase A gene and molecular genetics of metachromatic leucodystrophy.

This publication has 40 references indexed in Scilit:

• Simultaneous detection of the two most frequent metachromatic leukodystrophy mutations
  Human Genetics, 1993
• The organization of the gene for the human cerebroside sulfate activator protein
  FEBS Letters, 1991
• Population frequency of the arylsulphatase A pseudo-deficiency allele
  Human Genetics, 1991
• First‐trimester diagnosis of metachromatic leucodystrophy
  Clinical Genetics, 1988
• The Precursor of Sulfatide Activator Protein is Processed to Three Different Proteins
  Biological Chemistry Hoppe-Seyler, 1988
• Deleted ring chromosome 22 in a mentally retarded boy
  Clinical Genetics, 1986
• Multiple sulfatase deficiency: Degradation of arylsulfatase A and B after endocytosis in fibroblasts
  European Journal of Biochemistry, 1985
• Expression of human arylsulfatase-A in man-hamster somatic cell hybrids
  Cytogenetic and Genome Research, 1978
• A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM*
  Journal of Neurochemistry, 1963
• Zwei Typen von Cerebrosid-schwefelsäureestern als sog. „Prälipoide“ und Speichersubstanzen bei der Leukodystrophie, Typ Scholz (metachromatische Form der diffusen Sklerose)
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1958