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Paper Report for: Mizokami_2019_Intern.Med_58_2669

Reference

Title: Congenital Primary Hypothyroidism with the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-sized Thyroid Gland on Levothyroxine Replacement
Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J
Ref: Intern Med, 58:2669, 2019 : PubMed

        



Related information

Gene_Locus| human-TG
Mutation | A2362P_human-TG, K1393X_human-TG,



Citations formats

Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J (2019)
Congenital Primary Hypothyroidism with the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-sized Thyroid Gland on Levothyroxine Replacement
Intern Med 58: 2669-2673

Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J (2019)
Intern Med 58: 2669-2673



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