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Article

A novel OPTN variant causing PSP-CBS-like phenotype in familial amyotrophic lateral sclerosis.

Parkinsonism & related disorders - 1 Dec 2019

Stezin Albert, Chaithra S P, Holla Vikram V, Kamble Nitish, Yadav Ravi, Pal Pramod Kumar

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PMID: 31759189
DOI: 10.1016/j.parkreldis.2019.11.003

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A novel OPTN variant causing PSP-CBS-like phenotype in familial amyotrophic lateral sclerosis.PMID 31759189Read ↗

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OPTN variants in ALS cases: a case report of a novel mutation and literature review.Semantic proximity Read ↗

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Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.Semantic proximity Read ↗

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Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndromeSemantic proximity Read ↗

Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report.Semantic proximity Read ↗

A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany.Semantic proximity Read ↗

Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population.Semantic proximity Read ↗

Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China.Semantic proximity Read ↗

Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population.Semantic proximity Read ↗

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