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. Zhou; G. Yuan; G. Harifi; K. Cefle; S. Palanduz; H. Akoglu; P.J. 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

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Translated title of the contribution: 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. Zhou
, G. Yuan
, G. Harifi
, K. Cefle
, S. Palanduz

H. Akoglu, P.J. 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 journal › Article › Academic › peer-review

Translated title of the contribution	Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
Original language	Undefined/Unknown
Pages (from-to)	1175-1181
Number of pages	7
Journal	Human Mutation
Volume	33
Issue number	8
Publication status	Published - 2012

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/22553128

Cite this

Diggle, C. P., Parry, D. A., Logan, C. V., Laissue, P., Rivera, C., Restrepo, C. M., Fonseca, D. J., Morgan, J. E., Allanore, Y., Fontenay, M., Wipff, J., Varret, M., Gibault, L., Dalantaeva, N., Korbonits, M., Zhou, B., Yuan, G., Harifi, G., Cefle, K., ... Bonthron, D. T. (2012). Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis. Human Mutation, 33(8), 1175-1181. http://www.ncbi.nlm.nih.gov/pubmed/22553128

@article{ff8bbbaff1d7475e84738ad873ea0f8c,

title = "Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis",

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

year = "2012",

language = "Undefined/Unknown",

volume = "33",

pages = "1175--1181",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley \& Sons Inc.",

number = "8",

}

Diggle, CP, Parry, DA, Logan, CV, Laissue, P, Rivera, C, Restrepo, CM, Fonseca, DJ, Morgan, JE, Allanore, Y, Fontenay, M, Wipff, J, Varret, M, Gibault, L, Dalantaeva, N, Korbonits, M, Zhou, B, Yuan, G, Harifi, G, Cefle, K, Palanduz, S, Akoglu, H, Zwijnenburg, PJ, Lichtenbelt, KD, Aubry-Rozier, B, Superti-Furga, A, Dallapiccola, B, Accadia, M, Brancati, F, Sheridan, EG, Taylor, GR, Carr, IM, Johnson, CA, Markham, AF & Bonthron, DT 2012, 'Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis', Human Mutation, vol. 33, no. 8, pp. 1175-1181. <http://www.ncbi.nlm.nih.gov/pubmed/22553128>

TY - JOUR

T1 - Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

AU - Diggle, C.P.

AU - Parry, D.A.

AU - Logan, C.V.

AU - Laissue, P.

AU - Rivera, C.

AU - Restrepo, C.M.

AU - Fonseca, D.J.

AU - Morgan, J.E.

AU - Allanore, Y.

AU - Fontenay, M.

AU - Wipff, J.

AU - Varret, M.

AU - Gibault, L.

AU - Dalantaeva, N.

AU - Korbonits, M.

AU - Zhou, B.

AU - Yuan, G.

AU - Harifi, G.

AU - Cefle, K.

AU - Palanduz, S.

AU - Akoglu, H.

AU - Zwijnenburg, P.J.

AU - Lichtenbelt, K.D.

AU - Aubry-Rozier, B.

AU - Superti-Furga, A.

AU - Dallapiccola, B.

AU - Accadia, M.

AU - Brancati, F.

AU - Sheridan, E.G.

AU - Taylor, G.R.

AU - Carr, I.M.

AU - Johnson, C.A.

AU - Markham, A.F.

AU - Bonthron, D.T.

PY - 2012

Y1 - 2012

M3 - Article

SN - 1059-7794

VL - 33

SP - 1175

EP - 1181

JO - Human Mutation

JF - Human Mutation

IS - 8

ER -