Abstract
Helical mutations near the amino (N)-proteinase cleavage site have been suggested to result in a mixed osteogenesis imperfecta (OI)/Ehlers-Danlos syndrome (EDS) phenotype (Malfait et al.
Cite
CITATION STYLE
APA
Chen, H. (2016). Osteogenesis Imperfecta/Ehlers-Danlos Syndrome Overlap Syndrome. In Atlas of Genetic Diagnosis and Counseling (pp. 1–3). Springer New York. https://doi.org/10.1007/978-1-4614-6430-3_265-2
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