about
Infections of People with Complement Deficiencies and Patients Who Have Undergone SplenectomyInfectious diseases associated with complement deficiencies.Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeScreening for C3 deficiency in newborns using microarrays.Homozygous hereditary C3 deficiency due to a partial gene deletion.Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies.Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kindCarrier detection in families with properdin deficiency by microsatellite haplotyping.Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagenA novel mutation in the complement component 3 gene in a patient with selective IgA deficiency.Intrinsic differences between authentic and cryptic 5' splice sites.Hereditary deficiency of C3 in animals and humans.Genetic deficiencies of complement.Dysregulation of adaptive immune responses in complement C3-deficient patients.
P2860
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P2860
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Molecular basis of hereditary C3 deficiency.
@ast
Molecular basis of hereditary C3 deficiency.
@en
Molecular basis of hereditary C3 deficiency.
@nl
type
label
Molecular basis of hereditary C3 deficiency.
@ast
Molecular basis of hereditary C3 deficiency.
@en
Molecular basis of hereditary C3 deficiency.
@nl
prefLabel
Molecular basis of hereditary C3 deficiency.
@ast
Molecular basis of hereditary C3 deficiency.
@en
Molecular basis of hereditary C3 deficiency.
@nl
P2093
P2860
P356
P1476
Molecular basis of hereditary C3 deficiency.
@en
P2093
P2860
P304
P356
10.1172/JCI114821
P407
P50
P577
1990-10-01T00:00:00Z