Genetic dissection of autoimmune polyendocrine syndrome type 2: Common origin of a spectrum of phenotypes

Annals of the New York Academy of Sciences

Volumn 1110, Issue , 2007, Pages 159-165

  Ballarini, Annalisa ^a   Lee Kirsch, Min Ae ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

Addison's disease; APS2; Autoantibodies; Autoimmune disease; Autoimmune polyendocrine syndrome type 2; Autoimmune thyroid disease; Genetics; Type 1 diabetes

Indexed keywords

AUTOIMMUNE REGULATOR PROTEIN;

ADDISON DISEASE; AUTOIMMUNE DISEASE; AUTOIMMUNE POLYENDOCRINE SYNDROME TYPE 2; AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY; AUTOIMMUNITY; AUTOSOMAL RECESSIVE DISORDER; COMPREHENSION; CONFERENCE PAPER; DISEASE PREDISPOSITION; GENE MUTATION; GENETICS; HEREDITY; HUMAN; HYPOPARATHYROIDISM; INHERITANCE; INSULIN DEPENDENT DIABETES MELLITUS; MUCOCUTANEOUS CANDIDIASIS; MULTIPLE ENDOCRINE ADENOMATOSIS; PHENOTYPE; SYMPTOM; THEORY; THYROID DISEASE;

EID: 35748982635     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1196/annals.1423.018     Document Type: Conference Paper

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