Zhang, Yanqin
Ding, Jie
Funding for this research was provided by:
the National Key Research and Development Program of China The registry study of rare disease in children (2016YFC0901505)
the National Nature Science Foundation (81400685)
Beijing key laboratory of molecular diagnosis and study on pediatric genetic diseases (BZ0317)
Article History
Received: 6 February 2017
Revised: 1 August 2017
Accepted: 10 August 2017
First Online: 1 September 2017
Compliance with ethical standards
:
: The authors declare that they have no conflicts of interest