Skip to main content
Log in

Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism

  • Short Report
  • Published:
European Journal of Pediatrics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

References

  1. Hobart MJ, Fernie BA, DiScipio RG (1993) Structure of the human C6 gene. Biochemistry 32: 6198–6205

    CAS  PubMed  Google Scholar 

  2. Hobart MJ, Fernie BA, Fijen KAPMJ, Orren A (1998) The molecular basis of C6 deficiency in the Western Cape, South Africa. Hum Genet 103: 506–512

    Article  CAS  PubMed  Google Scholar 

  3. Newton JM, Cohen-Barak O, Hagiwara N, Gardner JM, Davisson MT, King RA, Brilliant MH (2001) Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. Am J Hum Genet 69: 981–988

    Google Scholar 

Download references

Acknowledgements

This work was supported in part by the Ankara Paediatric Disease Research Foundation, Ankara, Turkey; and partially by National Institutes of Health grant AR4596 to M.H.B. N.A.G. was supported by the MARC program grant T34 GM08718.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Aydan Ikinciogullari.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ikinciogullari, A., Tekin, M., Dogu, F. et al. Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism. Eur J Pediatr 164, 177–179 (2005). https://doi.org/10.1007/s00431-004-1582-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00431-004-1582-y

Keywords

Navigation