Literature DB >> 14974930

Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene.

Parth Narendran, Joaquin Lado-Abeal, Lars C Moeller, Samuel Refetoff.   

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Year:  2003        PMID： 14974930     DOI： 10.1046/j.1365-2265.2003.01924.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


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  1 in total

1.  A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.

Authors:  Alfonso Massimiliano Ferrara; Theodora Pappa; Jiao Fu; Christopher D Brown; April Peterson; Lars C Moeller; Kathleen Wyne; Kevin P White; Anna Pluzhnikov; Vassily Trubetskoy; Marcelo Nobrega; Roy E Weiss; Alexandra M Dumitrescu; Samuel Refetoff
Journal:  J Clin Endocrinol Metab       Date:  2015-01       Impact factor: 5.958
  1 in total

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