The American Journal of Human Genetics
Volume 99, Issue 1, 7 July 2016, Pages 236-245
ReportBi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
Under an Elsevier user license
open archive
Cited by (0)
© 2016 American Society of Human Genetics.