A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect

Journal of Clinical Endocrinology and Metabolism

Volumn 84, Issue 9, 1999, Pages 3248-3253

  Kosugi, Shinji ^a,c   Bhayana, Shelly ^b   Dean, Heather J ^b  

^a Department of Laboratory Medicine   (Japan)

^b UNIVERSITY OF MANITOBA   (Canada)

^c KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; IODIDE; PERCHLORATE; SODIUM ION; TECHNETIUM 99M; THYROTROPIN;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; FEMALE; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC COUNSELING; HETEROZYGOTE DETECTION; HOMOZYGOSITY; HUMAN; INTRON; IODIDE TRANSPORT DEFECT; MALE; NEWBORN SCREENING; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0033304901     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.84.9.3248     Document Type: Article

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