Associated Papers
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Minchiotti L et al.
Frontiers in Genetics, 2019
Acute infantile liver failure due to mutations in the TRMU gene.
Zeharia A et al.
American Journal of Human Genetics, 2009
An initiation codon mutation in CD18 in association with the moderate phenotype of leukocyte adhesion deficiency.
Sligh JE et al.
The Journal of Biological Chemistry, 1992
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