From bedside to the bench: a novel human homozygous IGF1R mutation is causal of abnormal skeletal acquisition

Manisha Dixit, Masanobu Fujimoto, Andrew Dauber, Vivian Hwa, Isabelle Maystadt, Anita Rauch, Jean De Schepper, Gozde Yildirim, Yanjiao Zhang, Shoshana Yakar

Research output: Contribution to journalMeeting abstract (Journal)

Original languageEnglish
Pages (from-to)315-315
JournalJournal of Bone and Mineral Research
Volume34
Publication statusPublished - Dec 2019

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