A Novel Mutation in theAlbuminGene (R218S) Causing Familial Dysalbuminemic Hyperthyroxinemia in a Family of Bangladeshi Extraction-Reference-Cited by-同舟云学术

A Novel Mutation in theAlbuminGene (R218S) Causing Familial Dysalbuminemic Hyperthyroxinemia in a Family of Bangladeshi Extraction

Author:

Greenberg Solomon Maximo¹,Ferrara Alfonso Massimiliano¹,Nicholas Everton S.²,Dumitrescu Alexandra M.¹,Cody Vivian³,Weiss Roy E.¹⁴,Refetoff Samuel¹⁴⁵

Affiliation:

1. Department of Medicine, The University of Chicago, Chicago, llinois.

2. Toronto East York General Hospital, Toronto, Canada.

3. Department of Structural Biology, Hauptman-Woodward Medical Research Institute, Buffalo, New York.

4. Department of Pediatrics, The University of Chicago, Chicago, llinois.

5. Department of Committee on Genetics, The University of Chicago, Chicago, llinois.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

Reference24 articles.

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