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Landers, John

One or more keywords matched the following items that are connected to Landers, John

Item Type	Name
Academic Article	The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.
Academic Article	A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.
Academic Article	The distinct genetic pattern of ALS in Turkey and novel mutations.
Academic Article	Comparative analysis of C9orf72 and sporadic disease in an ALS clinic population.
Academic Article	The role of de novo mutations in the development of amyotrophic lateral sclerosis.
Academic Article	Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
Academic Article	Modulation of actin polymerization affects nucleocytoplasmic transport in multiple forms of amyotrophic lateral sclerosis.
Concept	C9orf72 Protein
Academic Article	Genetic variability in sporadic amyotrophic lateral sclerosis.
Academic Article	Clinical testing panels for ALS: global distribution, consistency, and challenges.
Academic Article	Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.

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C9orf72 Protein