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A New Point Mutation C446r In The Thyroid Hormone Receptorbeta.
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It Resulted In Replacement Of The Normal Cysteine446 With An Arginine C446r That Has Not Been Previously Reported.
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Mps iiib is a rare disease affecting 5001000 people. Actions § 78, at 773. A new point mutation c446r in the thyroid hormone receptorbeta.
Truxton umsted, plaintiffs, appellants, v. Actions § 78, at 773. Fenwick margeson et al.
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