| 1 | FED, GP1BA, LCAT, PVWD
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| Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease.
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| Miller JL, Cunningham D, Lyle VA, Finch CN.
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| Proc Natl Acad Sci U S A 88(11):4761-5. 1991
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| 2 | FED, LCAT
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| Fish eye disease: a new familial condition with massive corneal opacities and dyslipoproteinaemia.
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| Carlson LA.
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| Eur J Clin Invest 12(1):41-53. 1982
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| 3 | FED, LCAT
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| Detection of heterozygotes for familial lecithin: cholesterol acyltransferase (LCAT) deficiency.
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| Frohlich J, Hon K, McLeod R.
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| Am J Hum Genet 34(1):65-72. 1982
|