Surprising news: A putative sulfate transporter is defective in Pendred's syndrome

European Journal of Endocrinology

Volumn 138, Issue 6, 1998, Pages 623-624

  Rutishauser, Jonas ^a   Kopp, Peter ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PENDRIN; UNCLASSIFIED DRUG;

CHROMOSOME 7Q; CLINICAL FEATURE; EAR MALFORMATION; GENE EXPRESSION; GENE MAPPING; GENETIC LINKAGE; GOITER; HUMAN; MOLECULAR CLONING; NORTHERN BLOTTING; PATHOGENESIS; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY; SYNDROME;

CARRIER PROTEINS; CHROMOSOMES, HUMAN, PAIR 7; COCHLEA; GOITER; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MEMBRANE TRANSPORT PROTEINS; MUTATION; SYNDROME; THYROID GLAND;

EID: 0031810527     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1380623     Document Type: Short Survey

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