Sklate, R T <br/><br/>
Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene.  [electronic resource] 

 -  Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme  Feb 2014 
 - 100-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1439-4286 
<br/><br/><label>Standard No.: </label>10.1055/s-0033-1358741  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Chromosomes, Human, X--genetics<br/>DNA--chemistry<br/>Female<br/>Genetic Diseases, X-Linked--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Prealbumin--chemistry<br/>Sequence Alignment<br/>Sequence Analysis, DNA<br/>Thyroxine--metabolism<br/>Thyroxine-Binding Globulin--chemistry