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

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Information Journal Paper

Title

Bardet-Biedl 9 Syndrome, A Rare Mutation

Pages

  153-156

Abstract

bardet-biedl syndrome (BBS) is a rare heterogenous autosomal recessive disease due to defects in primary cilia which until now, up to 21 types have been detected. A few reports of BBS in Iran have been published but this is the first type 9 genotyped and clinically discussed case. This type can cause severe and delayed onset renal failure.

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  • Cite

    APA: Copy

    NARIMANI, HOSSEIN. (2020). Bardet-Biedl 9 Syndrome, A Rare Mutation. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), 14(2), 153-156. SID. https://sid.ir/paper/762323/en

    Vancouver: Copy

    NARIMANI HOSSEIN. Bardet-Biedl 9 Syndrome, A Rare Mutation. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD)[Internet]. 2020;14(2):153-156. Available from: https://sid.ir/paper/762323/en

    IEEE: Copy

    HOSSEIN NARIMANI, “Bardet-Biedl 9 Syndrome, A Rare Mutation,” IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), vol. 14, no. 2, pp. 153–156, 2020, [Online]. Available: https://sid.ir/paper/762323/en

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