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Association of an Exon 3 Mutation (Trp66 → Gly) of the LDL Receptor with Variable Expression of Familial Hypercholesterolemia in a French Canadian Family

✍ Scribed by Emile Levy; Anne Minnich; Suzanne Lussier Cacan; Louise Thibault; Louise-Marie Giroux; Jean Davignon; Marie Lambert

No coin nor oath required. For personal study only.

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