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Hypobetalipoproteinemia with an apparently recessive inheritance due to a “de novo” mutation of apolipoprotein B

✍ Scribed by Sandra Lancellotti; Enza Di Leo; Junia Y. Penacchioni; Fiorella Balli; Laura Viola; Stefano Bertolini; Sebastiano Calandra; Patrizia Tarugi


Book ID
116270177
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
362 KB
Volume
1688
Category
Article
ISSN
0925-4439

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