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Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

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Year: 1996
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng0496-424
Authors: Val C. Sheffield, Zaki Kraiem, John C. Beck, Darryl Nishimura, Edwin M. Stone, Muhamad Salameh, Orit Sadeh, Benjamin Glaser
Institutions: University of Iowa, Technion – Israel Institute of Technology, Carmel Medical Center, Hadassah Medical Center
Language: English

Topic: Thyroid Disorders and Treatments
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Human Genome Research Institute
Awards: G3684147214, IMPROVED MUTATION DETECTION &HIGH THROUGHPUT GENOTYPING
OpenAlex ID: W2000184415
FWCI: 9.153
Cites: 27
Cited by: 164
Related to: 10
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