Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs
published in: European Journal of Paediatric Neurology
date of publication: 2014-08-07
main subject: Infantile neuronal ceroid lipofuscinosis, heterozygosity
Cites articles
There is nothing here
Article - wd:Q30872698