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Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, p. e82292
Journal Article
HUMAN MOLECULAR GENETICS, ISSN 0964-6906, 07/2019, Volume 28, Issue 13, pp. 2133 - 2142
Hereditary multiple osteochondromas (HMO) is a rare autosomal dominant skeletal disorder, caused by heterozygous variants in either EXT1 or EXT2, which encode... 
EXT1 | FGF | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | GENETICS & HEREDITY | PHENOTYPE | RISK | NATURAL-HISTORY
Journal Article
Human mutation, ISSN 1059-7794, 06/2019
Familial cerebral cavernous malformation (FCCM) is an autosomal dominant vascular disorder caused by heterozygous deleterious variants in KRIT1, CCM2 or... 
Journal Article
Expert Review of Clinical Immunology, ISSN 1744-666X, 2014, Volume 10, Issue 5, pp. 687 - 695
Rheumatoid arthritis (RA) is an autoimmune disease of unknown cause and a chronic and progressive inflammatory disorder ensuing in genetically predisposed... 
immune system | circadian | rhythm | clock gene | rheumatoid arthritis | RECEPTOR ROR-ALPHA | NECROSIS-FACTOR-ALPHA | IMMUNOLOGY | BLOOD MONONUCLEAR-CELLS | IMMUNE-SYSTEM | PERIPHERAL CIRCADIAN CLOCKS | LYMPHOCYTE SUBPOPULATIONS | GENE-EXPRESSION | REV-ERB-ALPHA | TNF-ALPHA | INFLAMMATORY CYTOKINES
Journal Article
Endocrine, ISSN 1355-008X, 12/2011, Volume 40, Issue 3, pp. 481 - 485
Journal Article
Oncology Letters, ISSN 1792-1074, 2017, Volume 14, Issue 1, pp. 23 - 30
Inactivating mutations of the multiple endocrine neoplasia 1 (MEN1) gene cause MEN1 syndrome, characterized by primary hyperparathyroidism (pHPT), and... 
Multiple endocrine neoplasia | MEN1 | Parathyroid carcinoma | PROTEIN | multiple endocrine neoplasia | ONCOLOGY | INTERACTS | MENI | PARAFIBROMIN | ENDOCRINE NEOPLASIA TYPE-1 | parathyroid carcinoma
Journal Article
Journal Article
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