Literature DB >> 8173

Diagnosis of inherited enzymatic deficiencies with tears: Fabry disease.

M A Del Monte, D L Johnson, E Cotlier, R J Desnick.   

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Year:  1976        PMID: 8173

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


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  2 in total

1.  Anderson-Fabry disease: rapid detection of carriers by hair bulb analysis.

Authors:  A Ejiofor; D Robinson; D Wise; M Hamers; J M Tager
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotes.

Authors:  A H Fensom; P F Benson; A R Grant; L Jacobs
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

  2 in total

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