A novel heterozygous NR1H4 termination codon mutation in idiopathic infantile cholestasis.
Chen, Xiu-Qi
A novel heterozygous NR1H4 termination codon mutation in idiopathic infantile cholestasis. [electronic resource] - World journal of pediatrics : WJP Feb 2012 - 67-71 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1867-0687
10.1007/s12519-011-0299-z doi
Asian People--genetics
Biomarkers--blood
Case-Control Studies
Cholestasis--genetics
Codon, Terminator--genetics
Diagnosis, Differential
Exons
Heterozygote
Humans
Infant
Mutation
Polymerase Chain Reaction
Prognosis
Receptors, Cytoplasmic and Nuclear--blood
A novel heterozygous NR1H4 termination codon mutation in idiopathic infantile cholestasis. [electronic resource] - World journal of pediatrics : WJP Feb 2012 - 67-71 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1867-0687
10.1007/s12519-011-0299-z doi
Asian People--genetics
Biomarkers--blood
Case-Control Studies
Cholestasis--genetics
Codon, Terminator--genetics
Diagnosis, Differential
Exons
Heterozygote
Humans
Infant
Mutation
Polymerase Chain Reaction
Prognosis
Receptors, Cytoplasmic and Nuclear--blood