Whole exome sequencing identified a novel COL2A1 mutation that causes mild Spondylo-epiphyseal dysplasia mimicking autosomal dominant brachyolmia
- Resource Type
- Academic Journal
- Source
- American Journal Of Medical Genetics - A. Mar 01, 2016 170(3):795-798
- Subject
- Language
- English
- ISSN
- 1552-4825