Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews.
about
Frameshift and splice-junction mutations in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis in Jews or Moroccan originInfectious diseases associated with complement deficiencies.Two novel mutations in the C7 gene in a Korean patient with complement C7 deficiency.Two distinct abnormalities in patients with C8 alpha-gamma deficiency. Low level of C8 beta chain and presence of dysfunctional C8 alpha-gamma subunit.Hereditary deficiency of the seventh component of complement and recurrent meningococcal infection: investigations of an Irish family using a novel haemolytic screening assay for complement activity and C7 M/N allotyping.
P2860
Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Hereditary complement deficien ...... in Sephardic (Moroccan) Jews.
@en
Hereditary complement deficien ...... C7/C8 deficiency in Sephardic
@nl
type
label
Hereditary complement deficien ...... in Sephardic (Moroccan) Jews.
@en
Hereditary complement deficien ...... C7/C8 deficiency in Sephardic
@nl
prefLabel
Hereditary complement deficien ...... in Sephardic (Moroccan) Jews.
@en
Hereditary complement deficien ...... C7/C8 deficiency in Sephardic
@nl
P2093
P1476
Hereditary complement deficien ...... in Sephardic (Moroccan) Jews.
@en
P2093
Ehrenfeld M
Rudensky B
P304
P577
1987-04-01T00:00:00Z