Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and CHCHD2[original query] |
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Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis. Journal of the neurological sciences 2016 Sep 368 389-91. Yang Xinglong, An Ran, Zhao Quanzhen, Zheng Jinhua, Tian Sijia, Chen Yalan, Xu Yanmi |
Identification of CHCHD2 mutations in patients with Alzheimer's disease, amyotrophic lateral sclerosis and frontotemporal dementia in China. Molecular medicine reports 2018 May . Liu Xixi, Jiao Bin, Zhang Weiwei, Xiao Tingting, Hou Lihua, Pan Chuzheng, Tang Beisha, Shen |
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy. Neurobiology of aging 2018 3 66 181.e1-181.e2. Rubino Elisa, Zhang Ming, Mongini Tiziana, Boschi Silvia, Vercelli Liliana, Vacca Alessandro, Govone Flora, Gai Annalisa, Giordana Maria Teresa, Grinberg Mark, Rogaeva Ekaterina, Rainero Innocen |
Frequency of Parkinson's Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study. Genes 2022 Jul 13 (8): . Vacchiano Veria, Bartoletti-Stella Anna, Rizzo Giovanni, Avoni Patrizia, Parchi Piero, Salvi Fabrizio, Liguori Rocco, Capellari Sabi |
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