Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.

Ouadani H, Ben-Mustapha I, Ben-ali M, Ben-khemis L, Larguèche B, Boussoffara R, Maalej S, Fetni I, Hassayoun S, Mahfoudh A, Mellouli F, Yalaoui S, Masmoudi H, Bejaoui M, Barbouche MR

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DOI: 10.1007/s00251-015-0878-6
Published: 2016 Jan
Container: Immunogenetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1007/s00251-015-0878-6,
  title = {Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.},
  author = {Ouadani H and Ben-Mustapha I and Ben-ali M and Ben-khemis L and Larguèche B and Boussoffara R and Maalej S and Fetni I and Hassayoun S and Mahfoudh A and Mellouli F and Yalaoui S and Masmoudi H and Bejaoui M and Barbouche MR},
  year = {2016},
  journal = {Immunogenetics},
  doi = {10.1007/s00251-015-0878-6},
  url = {https://doi.org/10.1007/s00251-015-0878-6}
}

RIS

TY  - JOUR
TI  - Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.
AU  - Ouadani H
AU  - Ben-Mustapha I
AU  - Ben-ali M
AU  - Ben-khemis L
AU  - Larguèche B
AU  - Boussoffara R
AU  - Maalej S
AU  - Fetni I
AU  - Hassayoun S
AU  - Mahfoudh A
AU  - Mellouli F
AU  - Yalaoui S
AU  - Masmoudi H
AU  - Bejaoui M
AU  - Barbouche MR
PY  - 2016
JO  - Immunogenetics
DO  - 10.1007/s00251-015-0878-6
UR  - https://doi.org/10.1007/s00251-015-0878-6
ER  -

APA

H, O., I, B., M, B., L, B., B, L., R, B., S, M., I, F., S, H., A, M., F, M., S, Y., H, M., M, B., & MR, B. (2016). Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.. Immunogenetics. https://doi.org/10.1007/s00251-015-0878-6

Source records

pubmed · retrieved 2026-11-10T12:01:46.327Z