Sequence-Based Analysis of Properdin Deficiency: Identification of Point Mutations in Two Phenotypic Forms of an X-Linked Immunodeficiency
Joakim Westberg, Gunilla Nordin Fredrikson, Lennart Truedsson, Anders G. Sjöholm, Mathias UhlénVolume:
29
Year:
1995
Pages:
9
DOI:
10.1006/geno.1995.1208
File:
PDF, 445 KB
1995