Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre)

Human Molecular Genetics

Volumn 7, Issue 7, 1998, Pages 1105-1112

  Coyle, Beth ^h   Reardon, William ^a   Herbrick, Jo Anne ^b   Tsui, Lap Chee ^b   Gausden, Eleanor ^h   Lee, Jeffrey ^b   Coffey, Rebecca ^a   Grueters, Annette ^c   Grossman, Ashley ^d   Phelps, Peter D ^e   Luxon, Linda ^f   Kendall Taylor, Pat ^g   Scherer, Stephen W ^b   Trembath, Richard C ^h  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c Charit Medical University   (Germany)

^d ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^e ROYAL NATIONAL THROAT NOSE AND EAR HOSPITAL   (United Kingdom)

^f UNIVERSITY COLLEGE LONDON   (United Kingdom)

^g ROYAL VICTORIA INFIRMARY   (United Kingdom)

^h UNIVERSITY OF LEICESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

IODIDE; THYROID HORMONE;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 7Q; FAMILY; GENE ISOLATION; GENE MUTATION; GOITER; HAPLOTYPE; HUMAN; PENDRED SYNDROME; PERCEPTION DEAFNESS; PRIORITY JOURNAL; THYROID HORMONE SYNTHESIS;

EID: 7144261720     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.7.1105     Document Type: Article

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