1972
DOI: 10.1016/s0140-6736(72)90355-8
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Hyperlipoproteinæmia Classification: The Optimum Routine Electrophoretic System and Its Relevance to Treatment

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Cited by 9 publications
(1 citation statement)
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“…Type I is an autosomal recessive disorder (Levy 1971). Type 11, also called familial hypercholesterolaemic xanthomatosis, is an autosomal dominant disorder (Christensen & Hdrder 1971, Levy 1971, Lehmann & Lines 1972. Type I1 is the only one where the familial incidence is so obvious that the autosomal dominance is clear (Christensen & H@rder 1971).…”
mentioning
confidence: 99%
“…Type I is an autosomal recessive disorder (Levy 1971). Type 11, also called familial hypercholesterolaemic xanthomatosis, is an autosomal dominant disorder (Christensen & Hdrder 1971, Levy 1971, Lehmann & Lines 1972. Type I1 is the only one where the familial incidence is so obvious that the autosomal dominance is clear (Christensen & H@rder 1971).…”
mentioning
confidence: 99%