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9. [Familial hypobetalipoproteinemia: Report of a family and review of Spanish contributions]. Diego Núñez MA; Cortijo González C An Esp Pediatr; 2002 Jan; 56(1):64-7. PubMed ID: 11792248 [TBL] [Abstract][Full Text] [Related]
10. Abetalipoproteinemia and homozygous hypobetalipoproteinemia: a framework for diagnosis and management. Lee J; Hegele RA J Inherit Metab Dis; 2014 May; 37(3):333-9. PubMed ID: 24288038 [TBL] [Abstract][Full Text] [Related]
11. Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia. Whitfield AJ; Marais AD; Robertson K; Barrett PH; van Bockxmeer FM; Burnett JR Hum Mutat; 2003 Aug; 22(2):178. PubMed ID: 12872264 [TBL] [Abstract][Full Text] [Related]
12. Homozygous familial hypobetalipoproteinemia: two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature. Cefalù AB; Norata GD; Ghiglioni DG; Noto D; Uboldi P; Garlaschelli K; Baragetti A; Spina R; Valenti V; Pederiva C; Riva E; Terracciano L; Zoja A; Grigore L; Averna MR; Catapano AL Atherosclerosis; 2015 Mar; 239(1):209-17. PubMed ID: 25618028 [TBL] [Abstract][Full Text] [Related]
13. Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1. Wakabayashi T; Takahashi M; Okazaki H; Okazaki S; Yokote K; Tada H; Ogura M; Ishigaki Y; Yamashita S; Harada-Shiba M; J Atheroscler Thromb; 2024 Jul; 31(7):1005-1023. PubMed ID: 38710625 [TBL] [Abstract][Full Text] [Related]
18. [Homozygous familial hypobetalipoproteinemia caused by APOB gene variations: a case report and review of literature]. Zhang YQ; Wang JS Zhonghua Er Ke Za Zhi; 2023 Jan; 61(1):70-75. PubMed ID: 36594125 [No Abstract] [Full Text] [Related]