宮本 範子
   Department   School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine
   Position   Assistant Professor
Article types Original article
Language English
Peer review Peer reviewed
Title A novel nucleotide mutation leading to a recurrent amino acid alteration in SH3BP2 in a patient with cherubism.
Journal Formal name:Congenit Anomalies (Kyoto)
Abbreviation:Congenit Anom (Kyoto)
Volume, Issue, Page 53,pp.166-169
Author and coauthor Sangu N†, Shimosato T, Inoda H, Shimada S, Shimojima K, Ando T, Yamamoto T*
Authorship Lead author
Publication date 2013
DOI 10.1111/cga.12013.