Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
Open Access
- 1 July 2003
- journal article
- other
- Published by BMJ in Journal of Medical Genetics
- Vol. 40 (7) , 90e-90
- https://doi.org/10.1136/jmg.40.7.e90
Abstract
No abstract availableKeywords
This publication has 0 references indexed in Scilit: