Two common and three novel PDS mutations in Thai patients with pendred syndrome

Journal of Endocrinological Investigation

Volumn 30, Issue 11, 2007, Pages 907-913

  Snabboon, Thiti ^a   Plengpanich, W ^a   Saengpanich, S ^a   Sirisalipoch, S ^a   Keelawat, S ^a   Sunthornyothin, S ^a   Khovidhunkit, W ^a   Suwanwalaikorn, S ^a   Sridama, V ^a   Shotelersuk, V ^a  

^a CHULALONGKORN UNIVERSITY   (Thailand)

Author keywords

Deafness; Discharge test; Goiter; PDS gene; Pendred syndrome; Perchlorate

Indexed keywords

GENE PRODUCT; PROTEIN PDS; UNCLASSIFIED DRUG; CARRIER PROTEIN; IODIDE; SLC26A4 PROTEIN, HUMAN;

ADULT; ALLELE; ARTICLE; CANCER RISK; CLINICAL ARTICLE; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC ANALYSIS; GOITER; HEARING IMPAIRMENT; HUMAN; HYPOTHYROIDISM; MALE; MISSENSE MUTATION; MOLECULAR GENETICS; MUTANT; ONCOCYTOMA; PENDRED SYNDROME; SEQUENCE ANALYSIS; THAILAND; THYROID FOLLICULAR CARCINOMA; ETHNOLOGY; GENETICS; METABOLISM; MIDDLE AGED; PEDIGREE; RISK FACTOR; SYNDROME; THYROID TUMOR;

ADENOMA, OXYPHILIC; ADULT; ALLELES; DEAFNESS; FEMALE; GOITER; HUMANS; HYPOTHYROIDISM; IODIDES; MALE; MEMBRANE TRANSPORT PROTEINS; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; RISK FACTORS; SYNDROME; THAILAND; THYROID NEOPLASMS;

EID: 40149103527     PISSN: 03914097     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF03349236     Document Type: Article

References (34)