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Human Molecular Genetics, ISSN 0964-6906, 1/2012, Volume 21, Issue 1, pp. 10 - 25
Journal Article
Nature Reviews Endocrinology, ISSN 1759-5029, 02/2017, Volume 13, Issue 2, pp. 105 - 124
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2016, Volume 12, Issue 3, p. e1005916
Journal Article
Journal Article
European journal of endocrinology, ISSN 0804-4643, 12/2017, Volume 177, Issue 6, pp. 485 - 501
Journal Article
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2011, Volume 6, Issue 1, pp. 78 - 78
Background: Anderson's Disease (AD)/Chylomicron Retention Disease (CMRD) is a rare hereditary hypocholesterolemic disorder characterized by a malabsorption... 
MEDICINE, RESEARCH & EXPERIMENTAL | SILVER-RUSSELL-SYNDROME | COMPLEX | EXPRESSION | VLDL-TRANSPORT VESICLE | Silver-Russell Syndrome - metabolism | Hypobetalipoproteinemias - metabolism | Humans | Asian Continental Ancestry Group - genetics | Child, Preschool | Male | Intestines - metabolism | Malabsorption Syndromes - metabolism | Silver-Russell Syndrome - genetics | Steatorrhea - genetics | Steatorrhea - metabolism | Endoscopy | Hypobetalipoproteinemias - pathology | Steatorrhea - pathology | Trisomy - pathology | Hypobetalipoproteinemias - genetics | Silver-Russell Syndrome - pathology | Monomeric GTP-Binding Proteins - genetics | Sequence Analysis, DNA | Malabsorption Syndromes - genetics | Chromosomes, Human, Pair 7 - metabolism | Phenotype | Trisomy - genetics | Uniparental Disomy - genetics | Monomeric GTP-Binding Proteins - metabolism | Biopsy | Monomeric GTP-Binding Proteins - chemistry | Mosaicism | Chromosomes, Human, Pair 7 - genetics | Malabsorption Syndromes - pathology | Uniparental Disomy - pathology | Care and treatment | Physiological aspects | Genetic aspects | Diagnosis | Apolipoproteins | Fabry's disease | Risk factors | Hypertension | Pediatrics | Plasma | Nutrition | Genes | Triglycerides | Light therapy | Medicine | Pathology | Lipoproteins | Diet | Vitamin E | Rodents | Growth hormones | Standard deviation | Mutation | Life Sciences | Genetics
Journal Article