Works matching IS 23146133 AND DT 2021 AND VI 2021

Results: 84
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    Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome.

    Published in:
    BioMed Research International, 2021, v. 2021, p. 1, doi. 10.1155/2021/6626015
    By:
    • Ali, Ghazanfar;
    • Sadia;
    • Jia Nee Foo;
    • Nasir, Abdul;
    • Chu-Hua Chang;
    • GuoYan Chew, Elaine;
    • Latif, Zahid;
    • Azeem, Zahid;
    • Ain-ul-Batool, Syeda;
    • Raza Kazmi, Syed Akif;
    • Awan, Naheed Bashir;
    • Khan, Abdul Hameed;
    • Fazal-Ur-Rehman;
    • Khalid, Madiha;
    • Wali, Abdul;
    • Sarwar, Samina;
    • Akhtar, Wasim;
    • Abbasi, Ansar Ahmed;
    • Nisar, Rameez
    Publication type:
    Article
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