Problems in Prenatal Diagnosis Using Sphingolipid Hydrolase Assays

Author:

Lowden J. Alexander,LaRamee Marie-Anne

Publisher

Springer US

Reference20 articles.

1. Crocker, A.C. The cerebral defect in Tay-Sachs disease and Niemann-Pick disease. J. Neurochem. 7: 69, (1961).

2. Brady, R.O., Kanfer, J.N., Mock, M.B. and Fredrickson, D.S. The metabolism of sphingomyelin, II. Evidence of an enzymatic deficiency in Niemann-Pick disease. Proc. Nat. Acad. Sci. U.S.A. 55: 366, (1966).

3. Schneider, R.B. and Kennedy, E.P. Sphingomyelinase in normal human spleens from subjects with Niemann-Pick disease. J. Lip. Res. 8: 202, (1967).

4. Lowden, J.A. and LaRamee, M.A. Sphingomyelinase in Type C Niemann-Pick disease. Arch. Neurol. Submitted, October 1971.

5. Spence, M.W. personal communication.

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