@article{6c279783a9f54c5eaa0b272e0bda8782,
title = "Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility",
keywords = "Primary osteoporosis, WNT1, PLS3, XYLT2, Osteogenesis imperfect, RECESSIVE OSTEOGENESIS IMPERFECTA, VAN-BUCHEM-DISEASE, WNT1 MUTATIONS, PEDIATRIC OSTEOPOROSIS, SOST GENE, PLASTIN 3, FAMILIES, DENSITY, PHENOTYPE, CHILDREN, 3121 General medicine, internal medicine and other clinical medicine",
author = "Makitie, {Riikka E.} and Kampe, {Anders J.} and Fulya Taylan and Outi Makitie",
year = "2017",
month = aug,
doi = "10.1007/s11914-017-0388-6",
language = "English",
volume = "15",
pages = "303--310",
journal = "Current Osteoporosis Reports (Online)",
issn = "1544-2241",
publisher = "Springer",
number = "4",
}