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A point mutation in the low density lipoprotein receptor gene that causes exon skipping and is associated with severe familial hypercholesterolemia (FH)

✍ Scribed by X.-M. Sun; D.D. Patel; S. McCarthy; B.L. Knight; A.K. Soutar

Book ID: 118325121
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 145 KB
Volume: 109
Category: Article
ISSN: 0021-9150
DOI: 10.1016/0021-9150(94)93450-9

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