Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular muscles
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Online |
Language: | English |
Published: |
Molecular Vision
2014
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888497/ |