Human Mutation

Cover image for Human Mutation

December 2006

Volume 27, Issue 12

Pages 1161–1243

  1. Editorial

    1. Top of page
    2. Editorial
    3. Review Articles
    4. Databases
    5. Research Articles
    1. You have free access to this content
  2. Review Articles

    1. Top of page
    2. Editorial
    3. Review Articles
    4. Databases
    5. Research Articles
    1. You have free access to this content
      Molecular approaches in the diagnosis of primary immunodeficiency diseases (pages 1163–1173)

      Maurizio Costabile, Alex Quach and Antonio Ferrante

      Article first published online: 7 SEP 2006 | DOI: 10.1002/humu.20412

    2. RAG-dependent primary immunodeficiencies (pages 1174–1184)

      Cristina Sobacchi, Veronica Marrella, Francesca Rucci, Paolo Vezzoni and Anna Villa

      Article first published online: 7 SEP 2006 | DOI: 10.1002/humu.20408

    3. You have free access to this content
      Activation-induced cytidine deaminase: structure–function relationship as based on the study of mutants (pages 1185–1191)

      Anne Durandy, Sophie Peron, Nadine Taubenheim and Alain Fischer

      Article first published online: 8 SEP 2006 | DOI: 10.1002/humu.20414

  3. Databases

    1. Top of page
    2. Editorial
    3. Review Articles
    4. Databases
    5. Research Articles
    1. You have free access to this content
      The IMGT/HLA and IPD databases (pages 1192–1199)

      James Robinson, Matthew J. Waller, Sylvie C. Fail and Steven G.E. Marsh

      Article first published online: 30 AUG 2006 | DOI: 10.1002/humu.20406

    2. Immunodeficiency mutation databases (IDbases) (pages 1200–1208)

      Hilkka Piirilä, Jouni Väliaho and Mauno Vihinen

      Article first published online: 26 SEP 2006 | DOI: 10.1002/humu.20405

    3. You have free access to this content
      BTKbase: the mutation database for X-linked agammaglobulinemia (pages 1209–1217)

      Jouni Väliaho, C.I. Edvard Smith and Mauno Vihinen

      Article first published online: 12 SEP 2006 | DOI: 10.1002/humu.20410

  4. Research Articles

    1. Top of page
    2. Editorial
    3. Review Articles
    4. Databases
    5. Research Articles
    1. Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase (pages 1218–1229)

      Dirk Roos, Martin de Boer, M. Yavuz Köker, Jan Dekker, Vinita Singh-Gupta, Anders Åhlin, Jan Palmblad, Özden Sanal, Magdalena Kurenko-Deptuch, Stephen Jolles and Baruch Wolach

      Article first published online: 13 SEP 2006 | DOI: 10.1002/humu.20413

    2. You have free access to this content

SEARCH

SEARCH BY CITATION