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Sequence-Based Analysis of Properdin Deficiency: Identification of Point Mutations in Two Phenotypic Forms of an X-Linked Immunodeficiency

✍ Scribed by Joakim Westberg; Gunilla Nordin Fredrikson; Lennart Truedsson; Anders G. Sjöholm; Mathias Uhlén


Book ID
115612770
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
445 KB
Volume
29
Category
Article
ISSN
0888-7543

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