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A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
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A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism. Thyroid. 2018 08; 28(8):1068-1070.
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PubMed
subject areas
Adolescent
Adult
Child
Congenital Hypothyroidism
Female
Goiter
Heterozygote
Humans
Male
Middle Aged
Mutation, Missense
Pedigree
Symporters
Young Adult
authors with profiles
Roy Emanuel Weiss