Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 8, 1998, Pages 2960-2963

  Carling, Tobias ^a   Correa, Pamela ^a   Hessman, Ola ^a   Hedberg, Jakob ^a   Skogseid, Britt ^a   Lindberg, Daniel ^a   Rastad, Jonas ^a   Westin, Gunnar ^a   Åkerström, Göran ^a  

^a UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; DNA; METHIONINE; PARATHYROID HORMONE; PROTEIN; SERUM ALBUMIN;

ADULT; AGED; ARTICLE; CHROMOSOME 11Q; CLINICAL ARTICLE; CONTROLLED STUDY; DELETION MUTANT; DISEASE SEVERITY; DNA SEQUENCE; FEMALE; FRAMESHIFT MUTATION; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERCALCEMIA; MALE; MISSENSE MUTATION; PARATHYROID ADENOMA; PARATHYROID HYPERPLASIA; PARATHYROID TUMOR; POSTMENOPAUSE; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL;

ADENOMA; AGED; AGED, 80 AND OVER; CHROMOSOMES, HUMAN, PAIR 11; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; HUMANS; HYPERPARATHYROIDISM; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; MUTATION; PARATHYROID HORMONE; PARATHYROID NEOPLASMS;

EID: 0031759392     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.83.8.2960     Document Type: Article

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