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 00099163. ISBN 13990004.

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