Hypobetalipoproteinemia with an apparently recessive inheritance due to a “de novo” mutation of apolipoprotein B
Autor: | Lancellotti, Sandra, Di Leo, Enza, Penacchioni, Junia Y., Balli, Fiorella, Viola, Laura, Bertolini, Stefano, Calandra, Sebastiano, Tarugi, Patrizia * |
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Zdroj: | In BBA - Molecular Basis of Disease 2004 1688(1):61-67 |
Databáze: | ScienceDirect |
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