Identification of a point mutation in growth factor repeat C of the low density lipoprotein-receptor gene in a patient with homozygous familial hypercholesterolemia that affects ligand binding and intracellular movement of receptors
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External Links
(P356) |
10.1073/PNAS.86.11.4166
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(P698) |
2726768
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(P819) |
1989PNAS...86.4166S
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(P932) |
287410
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(P5875) |
20429004
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