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Fish Eye Disease and LCAT-deficiency, extremes of one phenotype. A novel LCAT-mutation in a large family of Dutch descent

✍ Scribed by J.A. Kuivenhoven; H. Wiebusch; E. Van Voorst tot Voorst; J.S. Hill; P.H. Pritchard; H. Funke; J.J.P. Kastelein


Book ID
118325595
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
157 KB
Volume
109
Category
Article
ISSN
0021-9150

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