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A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein

✍ Scribed by H.K Jensen; H Holst; L.G Jensen; M.M Jørgensen; P.H Andreasen; T.G Jensen; B.S Andresen; F Heath; P.S Hansen; S Neve; K Kristiansen; O Færgeman; S Kølvraa; L Bolund; N Gregersen


Book ID
119436309
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
377 KB
Volume
131
Category
Article
ISSN
0021-9150

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