Additional file 2: of Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

Kausar, Mehran; Siddiqi, Saima; Yaqoob, Muhammad; Mansoor, Sajid; Makitie, Outi; Mir, Asif; Khor, Chiea; Foo, Jia; Anees, Mariam

doi:10.6084/m9.figshare.7356683.v1

12929_2018_481_MOESM2_ESM.docx (15.94 kB)

Additional file 2: 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 S2. Identification of a single homozygous segment on chr12 overlapping between all cases and none of the controls. (DOCX 15 kb)

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Agency for Science, Technology and Research, Singapore

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WNT signaling Whole-exome sequencing Osteoporosis Osteogenesis imperfecta

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Additional file 2: of Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

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