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Items: 2

1.
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
Y. Watanabe, E. Sharwood, B. Goodwin, M. K. Creech, H. Y. Hassan, M. G. Netea, M. Jaeger, A. Dumitrescu, S. Refetoff, T. Huynh, R. E. Weiss
BMC Med Genet. 2018; 19: 69. Published online 2018 May 2. doi: 10.1186/s12881-018-0588-7
PMCID:
PMC5932782
AbstractArticlePDF–1.5M
2.
CMPD: cancer mutant proteome database
Po-Jung Huang, Chi-Ching Lee, Bertrand Chin-Ming Tan, Yuan-Ming Yeh, Lichieh Julie Chu, Ting-Wen Chen, Kai-Ping Chang, Cheng-Yang Lee, Ruei-Chi Gan, Hsuan Liu, Petrus Tang
Nucleic Acids Res. 2015 Jan 28; 43(Database issue): D849–D855. Published online 2014 Nov 14. doi: 10.1093/nar/gku1182
PMCID:
PMC4383976
AbstractArticlePDF–1.8M

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