Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations.
Di Leo E; Magnolo L; Bertolotti M; Bourbon M; Carmo Pereira S; Pirisi M; Calandra S; Tarugi P; Clinical Genetics, 2008, vol. 74, issue 3, p 267, ISSN 13990004. ISBN 13990004.

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