Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

C.P. Diggle, D.A. Parry, C.V. Logan, P. Laissue, C. Rivera, C.M. Restrepo, D.J. Fonseca, J.E. Morgan, Y. Allanore, M. Fontenay, J. Wipff, M. Varret, L. Gibault, N. Dalantaeva, M. Korbonits, B.W. Zhou, G. Yuan, G. Harifi, K. Cefle, S. PalanduzH. Akoglu, P.J.G. Zwijnenburg, K.D. Lichtenbelt, B. Aubry-Rozier, A. Superti-Furga, B. Dallapiccola, M. Accadia, F. Brancati, E.G. Sheridan, G.R. Taylor, I.M. Carr, C.A. Johnson, A.F. Markham, D.T. Bonthron

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1175-1181
JournalHuman Mutation
Volume33
Issue number8
DOIs
Publication statusPublished - 2012

Cite this

Diggle, C. P., Parry, D. A., Logan, C. V., Laissue, P., Rivera, C., Restrepo, C. M., ... Bonthron, D. T. (2012). Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis. Human Mutation, 33(8), 1175-1181. https://doi.org/10.1002/humu.22111