Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes

Journal of Clinical Endocrinology and Metabolism

Volumn 94, Issue 11, 2009, Pages 4517-4523

  Triolo, Taylor M ^a   Baschal, Erin E ^a   Armstrong, Taylor K ^a   Toews, Carrie S ^a   Fain, Pamela R ^a   Rewers, Marian J ^a   Yu, Liping ^a   Miao, Dongmei ^a   Eisenbarth, George S ^a   Gottlieb, Peter A ^a   Barker, Jennifer M ^a  

^a UNIVERSITY OF COLORADO DENVER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; STEROID 21 MONOOXYGENASE;

ADRENAL INSUFFICIENCY; ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; DISEASE COURSE; FEMALE; FOLLOW UP; GENETIC IDENTIFICATION; GENOTYPE; HIGH RISK PATIENT; HOMOZYGOSITY; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; PATIENT IDENTIFICATION; PRIORITY JOURNAL; PROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 70449107613     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2009-1308     Document Type: Article

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