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A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease

✍ Scribed by S. Bertolini; L. Pisciotta; M. Seri; R. Cusano; A. Cantafora; L. Calabresi; G. Franceschini; R. Ravazzolo; S. Calandra

Book ID: 119434024
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 179 KB
Volume: 154
Category: Article
ISSN: 0021-9150
DOI: 10.1016/s0021-9150(00)00587-6

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