Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease.
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Germain DP, Salard D, Fellmann F, Azibi K, Caillaud C, Bernard MC, Poenaru L
Identification of a novel de novo mutation (G373D) in the alpha-galactosidase A gene (GLA) in a patient affected with Fabry disease.
Hum Mutat. 2001 Apr;17(4):353.
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- 11295840 [ View in PubMed]
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