Associated Papers
A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype.
Radha Rama Devi A et al.
Clinical Genetics, 2021
Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.
Sato Y et al.
The Journal of Biological Chemistry, 2008
Select a paper to view details