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European Journal of Human Genetics, ISSN 1018-4813, 08/2016, Volume 24, Issue 9, pp. 1274 - 1279
.... Although successfully used to facilitate the diagnosis of single-gene disorders, the genetic cause... 
EXOME | SECONDARY HYPOCALCEMIA | FAMILIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | DISORDERS | MUTATIONS | TRPM6 | THYROGLOBULIN GENE | DISCOVERY | GENOME | HYPOMAGNESEMIA | Intestinal Diseases - complications | Lipid Metabolism, Inborn Errors - genetics | Lipoproteins - genetics | Humans | Hypothyroidism - complications | Male | Magnesium Deficiency - diagnosis | Young Adult | Magnesium Deficiency - genetics | Magnesium Deficiency - complications | RNA Splicing | Female | Hypothyroidism - genetics | Phytosterols - adverse effects | Lipid Metabolism, Inborn Errors - diagnosis | Intestinal Diseases - genetics | Hypothyroidism - diagnosis | Phytosterols - genetics | Intestinal Diseases - diagnosis | Phenotype | Pedigree | Adolescent | Hypercholesterolemia - diagnosis | Thyroglobulin - genetics | TRPM Cation Channels - genetics | Hypercholesterolemia - complications | Consanguinity | Hypercholesterolemia - genetics | Lipid Metabolism, Inborn Errors - complications | Mutation | ATP Binding Cassette Transporter, Sub-Family G, Member 5 - genetics | Alternative splicing | Pediatrics | Phenotypes | Congenital diseases | Internal medicine | Genomes | Thyroid gland | Sitosterolemia | Hypothyroidism | Patients | Medicine | Transient receptor potential proteins | Hypercholesterolemia | Sterols | Thyroglobulin | Atherosclerosis | Genetics | Magnesium | Diagnosis | Bioinformatics | Hypomagnesemia | Genotypes
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 01/2010, Volume 130, Issue 1, pp. 93 - 101
Journal Article
Journal Article
Journal Article
Journal of Autoimmunity, ISSN 0896-8411, 2007, Volume 28, Issue 2, pp. 85 - 98
.... Indeed, several AITD susceptibility genes have been identified. Some of these susceptibility genes are specific to either Graves... 
Allergy and Immunology | Genetics | Organ specific autoimmunity | Immunoregulation | Autoimmune thyroiditis | COLLAGEN-INDUCED ARTHRITIS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | SINGLE-NUCLEOTIDE POLYMORPHISM | MAJOR HISTOCOMPATIBILITY COMPLEX | HUMAN B-LYMPHOCYTES | IMMUNOLOGY | LYMPHOID TYROSINE PHOSPHATASE | genetics | PRIMARY HORMONOGENIC SITES | autoimmune thyroiditis | immunoregulation | organ specific autoimmunity | VASCULAR ENDOTHELIAL-CELLS | DIABETES SUSCEPTIBILITY GENES | MHC CLASS-II | Antigens, CD - immunology | Receptors, Thyrotropin - genetics | Graves Disease - etiology | Thyroglobulin - metabolism | Humans | Protein Tyrosine Phosphatases - metabolism | Antigens, CD - genetics | Antigens, CD - metabolism | Graves Disease - genetics | Hashimoto Disease - immunology | Protein Tyrosine Phosphatases - genetics | CD40 Antigens - metabolism | Graves Disease - immunology | Antigens, Differentiation - metabolism | CD40 Antigens - genetics | Hashimoto Disease - etiology | Genetic Predisposition to Disease | Hashimoto Disease - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 22 | Receptors, Thyrotropin - metabolism | CTLA-4 Antigen | Animals | Thyroglobulin - genetics | Antigens, Differentiation - genetics | Polymorphism, Single Nucleotide | Antigens, Differentiation - immunology | Autoimmunity | Genetic research | Development and progression | Thyroid diseases
Journal Article
Journal Article