A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report

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Publication year
2018
Author(s)
Watanabe, Y.
Sharwood, E.
Goodwin, B.
Creech, M.K.
Hassan, H.Y.
Netea, M.G.
Jaeger, M.
Huynh, T.
Weiss, R.
Source
BMC Medical Genetics, 19, (2018), pp. |, article 69
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/191405   https://hdl.handle.net/2066/191405
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