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4. Mental retardation and ataxia due to normotriglyceridemic hypobetalipoproteinemia. Homer VM; George PM; du Toit S; Davidson JS; Wilson CJ Ann Neurol; 2005 Jul; 58(1):160-3. PubMed ID: 15984016 [TBL] [Abstract][Full Text] [Related]
5. Genetic aspects of disorders in beta-lipoproteins. Levy E; Seidman EG J Pediatr Gastroenterol Nutr; 1992 May; 14(4):472-3. PubMed ID: 1517954 [No Abstract] [Full Text] [Related]
6. [The role of ascorbic acid, tocopherol and retinol in the processes of carcinogenesis]. Wartanowicz M; Potrzebnicka K Wiad Lek; 1988 Apr; 41(8):507-13. PubMed ID: 3070954 [No 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. Fatty infiltration of the liver in a case of hypobetalipoproteinaemia with a novel mutation in the APOB gene. Florkowski C; Hedley J; Bickley V; Hooper AJ; Burnett JR; George P N Z Med J; 2010 Mar; 123(1310):98-100. PubMed ID: 20360784 [No Abstract] [Full Text] [Related]
13. Donor splice-site mutation (210+1G_C) in the ApoB gene causes a very low level of ApoB-100 and LDL cholesterol. Welty FK; Guida KA; Andersen JJ Arterioscler Thromb Vasc Biol; 2001 Nov; 21(11):1864-5. PubMed ID: 11701479 [No Abstract] [Full Text] [Related]
14. [A case of familial hypo-beta-lipoproteinemia with steatosis of the liver]. Ohnishi S; Kodama T; Kanamori H; Moriyama T; Iwasaki Y; Itakura H; Ohkubo A; Takaku F; Fukusato T; Aburatani H Nihon Naika Gakkai Zasshi; 1984 May; 73(5):676-9. PubMed ID: 6491443 [No Abstract] [Full Text] [Related]
15. Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation. Pulai JI; Zakeri H; Kwok PY; Kim JH; Wu J; Schonfeld G Am J Med Genet; 1998 Nov; 80(3):218-20. PubMed ID: 9843041 [TBL] [Abstract][Full Text] [Related]