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|Title:||Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function|
Anderson, Lisa K.
Keith, Patrick A.
Rondon Galeano, Maria C.
Childrens Hospital Westmead: Paediatrics & Child Health
|Publisher:||Nature Publishing Group|
|Citation:||Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function, Scientific Reports, vol.6, N/A, 2016,pp 1-10|
|Department/Unit/Centre:||Childrens Hospital Westmead: Paediatrics & Child Health|
|Disclaimer:||This work has been made available to the staff and students of the University of Sydney for the purposes of research and study only. It constitutes material that is held by the University for the purposes of reporting for HERDC and the ERA. This work may not be downloaded, copied and distributed to any third party .|
|Type:||C1 - Refereed Journal articles|
|Appears in Collections:||University of Sydney Research Outputs|
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