Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.
- 1 May 1973
- journal article
- Vol. 25 (3) , 287-93
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
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- Prenatal Diagnosis of Tay-Sachs GenotypesBMJ, 1971
- Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytesThe Journal of Pediatrics, 1971
- Tay-Sachs Disease: Prenatal DiagnosisScience, 1971
- Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase AThe Journal of Pediatrics, 1970
- Tay-Sachs DiseaseNew England Journal of Medicine, 1970
- Identification of tay-sachs disease carriers by acrylamide gel electrophoresisClinica Chimica Acta; International Journal of Clinical Chemistry, 1970
- PRENATAL DIAGNOSIS OF TAY-SACHS DISEASEThe Lancet, 1970
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969