Literature DB >> 22448464

Severe primary antibody deficiency due to a novel mutation of mu heavy chain.

I Mohammadzadeh1, M Yeganeh, A Aghamohammadi, N Parvaneh, N Behniafard, H Abolhassani, F Tabassomi, M Hemmat, H Kanegane, T Miyawaki, O Ohara, N Rezaei.   

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Year:  2012        PMID： 22448464

Source DB:  PubMed          Journal:  J Investig Allergol Clin Immunol        ISSN： 1018-9068            Impact factor:   4.333


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  1 in total

1.  Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene.

Authors:  P Silva; A Justicia; A Regueiro; S Fariña; J M Couselo; L Loidi
Journal:  Genes Immun       Date:  2017-08-03       Impact factor: 2.676
  1 in total

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