SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.

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SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.

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http://www.wikidata.org/entity/Q55313288

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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SPG11 mutations cause widespre ...... ut restricted cortical damage.

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SPG11 mutations cause widespre ...... ut restricted cortical damage.

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SPG11 mutations cause widespre ...... ut restricted cortical damage.

@en

SPG11 mutations cause widespre ...... ut restricted cortical damage.

@nl

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SPG11 mutations cause widespre ...... ut restricted cortical damage.

@en

SPG11 mutations cause widespre ...... ut restricted cortical damage.

@nl

P1476

SPG11 mutations cause widespre ...... but restricted cortical damage

@en

P2093

Alberto Rolim Muro Martinez

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Carlos Roberto Martins

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Celeste Montecchiani

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Charles Marques Lourenço

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Ingrid Faber

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Marcondes Cavalcante França

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Melina Pazian Martins

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Orlando Graziani Povoas Barsottini

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Thiago Junqueira Ribeiro de Rezende

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Wilson Marques

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P2860

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Energy defects in Huntington's disease: Why "in vivo" evidence matters.

Multi-contrast multi-atlas parcellation of diffusion tensor imaging of the human brain

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

Classification of the hereditary ataxias and paraplegias.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

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848-857

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scholarly article

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10.1016/J.NICL.2018.05.031

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P478

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Antonio Orlacchio

José Luiz Pedroso

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2018-06-09T00:00:00Z

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29946510

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6008284

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