Haluk Caliskan
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View article: Clinical heterogeneity within the <scp>ALS‐FTD</scp> spectrum in a family with a homozygous optineurin mutation
Clinical heterogeneity within the <span>ALS‐FTD</span> spectrum in a family with a homozygous optineurin mutation Open
Objective Mutations in the gene encoding for optineurin ( OPTN ) have been reported in the context of different neurodegenerative diseases including the amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) spectrum. Based …
View article: Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder
Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder Open