- Title
- Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report
- Creators
- Fatemeh Maghami - Shiraz, IranSeyed Mohammad Bagher Tabei - Shiraz, IranHossein Moravej - Shiraz, IranHassan Dastsooz - Persian BayanGene Research and Training Center, Dr. Faghihi’s Medical Genetics Center, Shiraz, IranFarzaneh Modarresi - 1501 NW 10th Ave, BRB 508, Miami, FL 33136 USAMohammad Silawi - Persian BayanGene Research and Training Center, Dr. Faghihi’s Medical Genetics Center, Shiraz, IranMohammad Ali Faghihi - Persian BayanGene Research and Training Center, Dr. Faghihi’s Medical Genetics Center, Shiraz, Iran
- Publication Details
- BMC medical genetics, Vol.19(1), pp.86-86
- Publisher
- BioMed Central; London
- Grant note
- R01NS081208-01A1 / ; NB0223 / ;
- Academic Unit
- Miller School of Medicine; UMMG Dept of Psychiatry & Behavioral Sciences
- Language
- English
- Resource Type
- Journal article
- PMID
- 29801479
- PMCID
- PMC5970456
- Record Identifier
- 991031576586802976
Journal article
Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report
BMC medical genetics, Vol.19(1), pp.86-86
2018-05-25
PMCID: PMC5970456
PMID: 29801479
Metrics
19 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.132 Extracellular Matrix & Cell Differentiation
- 1.132.1065 Osteogenesis Imperfecta
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites