TY  - JOUR

T1  - Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect.

JO  - Journal of Clinical Endocrinology and Metabolism

UR  - https://eprints.whiterose.ac.uk/id/eprint/114458

PY  - 2017/03/16

AU  - Webb EA

AU  - Balasubramanian M

AU  - Fratzl-Zelman N

AU  - Cabral WA

AU  - Titheradge H

AU  - Alsaedi A

AU  - Saraff V

AU  - Vogt J

AU  - Cole T

AU  - Stewart S

AU  - Crabtree NJ et al

ED  - 

DO  - DOI: 10.1210/jc.2016-3766

PB  - Endocrine Society

VL  - 102

IS  - 6

SP  - 2019

EP  - 2028

Y2  - 2025/11/06

ER  -