مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

TRIFUNCTIONAL PROTEIN DEFICIENCY DUE TO HADHB MUTATIONS IS A MULTISYSTEM, β-OXIDATION DISORDER (LETTER TO THE EDITOR)

Pages

  767-769

Keywords

Not Registered.

Abstract

 Dear Editor, With interest, we read the article by Shahrokhi et al about a new-born with a β-oxidation defect due to a mutation in the HADHB gene encoding the β-subunit of the trifunctional protein. 1 We have the following comments and concerns. A main disadvantage of the study is that the pathogenicity of the HADHB mutation was confirmed only by in silico techniques...

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  • Cite

    APA: Copy

    FINSTERER, JOSEF, & ZARROUK MAHJOUB, SINDA. (2017). TRIFUNCTIONAL PROTEIN DEFICIENCY DUE TO HADHB MUTATIONS IS A MULTISYSTEM, β-OXIDATION DISORDER (LETTER TO THE EDITOR). ARCHIVES OF IRANIAN MEDICINE, 20(12), 767-769. SID. https://sid.ir/paper/281599/en

    Vancouver: Copy

    FINSTERER JOSEF, ZARROUK MAHJOUB SINDA. TRIFUNCTIONAL PROTEIN DEFICIENCY DUE TO HADHB MUTATIONS IS A MULTISYSTEM, β-OXIDATION DISORDER (LETTER TO THE EDITOR). ARCHIVES OF IRANIAN MEDICINE[Internet]. 2017;20(12):767-769. Available from: https://sid.ir/paper/281599/en

    IEEE: Copy

    JOSEF FINSTERER, and SINDA ZARROUK MAHJOUB, “TRIFUNCTIONAL PROTEIN DEFICIENCY DUE TO HADHB MUTATIONS IS A MULTISYSTEM, β-OXIDATION DISORDER (LETTER TO THE EDITOR),” ARCHIVES OF IRANIAN MEDICINE, vol. 20, no. 12, pp. 767–769, 2017, [Online]. Available: https://sid.ir/paper/281599/en

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