Whole‐exome sequencing detects somatic mutations of <i>IDH1</i> in metaphyseal chondromatosis with <scp>D</scp>‐2‐hydroxyglutaric aciduria (MC‐HGA)
Lisenka E.L.M. Vissers(Radboud University Nijmegen), Andrea Superti‐Furga(University of Lausanne), Joris A. Veltman(Edinburgh Cancer Research), Virginia Fano(Garrahan Hospital), Han G. Brunner(Radboud University Nijmegen), Gen Nishimura(Musashino University), Ahmet Dursun(Zonguldak Bülent Ecevit University), Jörn Oliver Sass(Boston Children's Hospital), Luisa Bonafé(University of Lausanne), Tae‐Joon Cho(Seoul National University Children's Hospital), Sheila Unger(University of Lausanne), Giuseppina Timpani(Azienda Ospedaliera S.Maria), Diego Martinelli(Bambino Gesù Children's Hospital), Carlo Dionisi‐Vici(Bambino Gesù Children's Hospital), Sun Hee Lee(Inje University Busan Paik Hospital), Domenico Barbuti(Bambino Gesù Children's Hospital), Ok Hwa Kim(Ajou University Hospital), Belinda Campos‐Xavier(University of Lausanne)
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