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Paper Report for: Watanabe_2018_BMC.Med.Genet_19_69

Reference

Title: A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S and Weiss RE <1 more author(s)>
Ref: BMC Med Genet, 19:69, 2018 : PubMed

        



Related information

Gene_Locus| human-TG
Mutation | G2341S_human-TG,



Citations formats

Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S, Huynh T, Weiss RE (2018)
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
BMC Med Genet 19: 69

Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S, Huynh T, Weiss RE (2018)
BMC Med Genet 19: 69



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