Published in
BioMed Central, BMC Medical Genetics, 1(19), 2018
DOI: 10.1186/s12881-018-0588-7
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A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
Journal article published in 2018 by
Y. Watanabe,
E. Sharwood,
R. E. Weiss 
,
B. Goodwin,
M. K. Creech,
Creech Mk,
H. Y. Hassan,
Hassan Hy,
Netea Mg,
M. G. Netea,
M. Jaeger ,
A. Dumitrescu,
S. Refetoff,
T. Huynh,
Weiss Re
,
B. Goodwin,
M. K. Creech,
Creech Mk,
H. Y. Hassan,
Hassan Hy,
Netea Mg,
M. G. Netea,
M. Jaeger ,
A. Dumitrescu,
S. Refetoff,
T. Huynh,
Weiss Re
This paper is made freely available by the publisher.
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