WHIM Syndrome-linked CXCR4 mutations drive osteoporosis

Anginot, A; Nguyen, J; Abou Nader, Z; Rondeau, V; Bonaud, A; Kalogeraki, M; Boutin, A; Lemos, JP; Bisio, V; Koenen, J; Sakr, LHD; Picart, A; Coudert, A; Provot, S; Dulphy, N; Aurrand-Lions, M; Mancini, SJC; Lazennec, G; McDermott, DH; Guidez, F; Blin-Wakkach, C; Murphy, PM; Cohen-Solal, M; Espéli, M; Rouleau, M; Balabanian, K

Balabanian, K (通讯作者)，CNRS, Microenvironm Tumor Niches GDR3697, Micronit, France.;Balabanian, K (通讯作者)，Univ Paris Cite, Inst Rech St Louis, INSERM, U1160, Paris, France.;Balabanian, K (通讯作者)，Hop St Louis, OPALE Carnot Inst, Org Partnerships Leukemia, Paris, France.

NATURE COMMUNICATIONS, 2023; 14 (1):

Abstract

WHIM Syndrome is a rare immunodeficiency caused by gain-of-function CXCR4 mutations. Here we report a decrease in bone mineral density in 25% of WHIM ......

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