University of Münster
CRIS@UM
DE | EN

A homozygous intronic branch-point deletion in the ALPL gene causes infantile hypophosphatasia.

Mentrup B, Girschick H, Jakob F, Hofmann C

Research article (journal) | Peer reviewed

Details about the publication

Journal: Bone
Volume: 94
Page range: 75-83
Status: Published
Release year: 2017
Language in which the publication is written: English
DOI: 10.1016/j.bone.2016.10.022.

Authors from the University of Münster

Mentrup, Birgit
Institute of Musculoskeletal Medicine (IMM)