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Additional file 3: of Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

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posted on 2018-11-17, 05:00 authored by Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Khor, Jia Foo, Mariam Anees
Table S3. List of rare homozygous variants in III:5 and III:15 located within the shared homozygous segment on chr12. (DOCX 13 kb)

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Agency for Science, Technology and Research, Singapore

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    Journal of Biomedical Science

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    Keywords

    WNT signalingWhole-exome sequencingOsteoporosisOsteogenesis imperfecta

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