Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling

Author： Origone Paola  

Publisher： Informa Healthcare

ISSN： 2167-8421

Source： Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol.14, Iss.5-6, 2013-09, pp. : 479-480

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

C9orf72 repeat expansions are a rare genetic cause of parkinsonism

By Lesage Suzanne  

Brain, Vol. 136, Iss. 2, 2013-02 ,pp. : 385-391

Oxford University Press

Access to resources Recommend Favorite

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

By Simn-Snchez Javier  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 723-735

Oxford University Press

Access to resources Recommend Favorite

C9orf72 repeat expansions are not detected in Chinese patients with familial ALS

By Liu Rong   Tang Lu   Cai Bin   Liu Xiaolu   Ye Shan   Ma Yan   Zhang Huagang   Fan Dongsheng  

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 7-8, 2013-12 ,pp. : 630-631

Informa Healthcare

Access to resources Recommend Favorite

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

By Chi Adriano  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 784-793

Oxford University Press

Access to resources Recommend Favorite

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

By Boeve Bradley F.  

Brain, Vol. 135, Iss. 3, 2012-04 ,pp. : 765-783

Oxford University Press

Access to resources Recommend Favorite