Missense mutations in the arylsulphatase a genes of metachromatic leukodystrophy patients

INIS

• mutations 100%
• patients 83%
• exons 50%
• proteins 33%
• genes 33%
• amino acids 33%
• adults 16%
• diseases 16%
• nucleotides 16%
• tyrosine 16%
• point mutations 16%
• juveniles 16%
• alanines 16%
• lysine 16%
• serine 16%
• glutamic acid 16%
• valine 16%

Biochemistry, Genetics and Molecular Biology

• Mutation 83%
• Metachromatic Leukodystrophy 83%
• Nested Gene 33%
• Arylsulfatase A 33%
• Position 33%
• Serine 16%
• Missense Mutation 16%
• Valine 16%
• Glutamic Acid 16%
• Lysine 16%
• Alanine 16%
• Point Mutation 16%
• Arylsulfatase 16%

Neuroscience

• Arylsulfatase 16%