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      Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.

      The New England journal of medicine

      Amino Acid Sequence, Child, DNA Fingerprinting, Germ-Line Mutation, Humans, Hyperthyroidism, congenital, genetics, Infant, Newborn, Male, Molecular Sequence Data, Receptors, Thyrotropin, Transfection

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          7800007
          10.1056/NEJM199501193320304

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