The use of tears for heterozygote detection and genetic counseling

Research output: Contribution to journalArticlepeer-review

Abstract

The impressive results with tear enzyme determinations in Tay Sachs' and Fabry's disease suggest that all inborn errors of metabolism with known enzyme deficiencies should be studied similarly. It may eventually be possible for such tests to provide the type of information necessary for the prevention of the many inborn errors of metabolism that affect man.

Original languageEnglish (US)
Pages (from-to)159-160
Number of pages2
JournalInvestigative ophthalmology
Volume13
Issue number3
StatePublished - Jan 1 1974
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

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