Mutation analysis in patients with the typical form of Anderson-Fabry disease.

doi:10.1093/hmg/2.7.1051

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Mutation analysis in patients with the typical form of Anderson-Fabry disease.

Human molecular genetics - 1 Jul 1993

Davies J P, Winchester B G, Malcolm S

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Share to alpha-Galactosidase
Share to Amino Acid Sequence
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 8395937
DOI: 10.1093/hmg/2.7.1051

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