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SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China

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Acknowledgments

We are grateful to all of the subjects for their participation in our study. This work was supported by the National Natural Sciences Foundation of China (No: 30971034, 81171068, 81100845) and the Project in the Major State Basic Research Development Program of China (973 Program) (2011CB510000).

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Correspondence to Juan Du.

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On behalf of all authors, the corresponding author states that there is no conflict of interest.

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All human studies have been approved by the appropriate ethics committee and have, therefore, been performed in accordance with the ethical standards laid down in 1964 Declaration of Helsinki and its later amendments. All persons gave their informed consent prior to their inclusion in the study.

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Yang, Y., Zhou, Z., Liao, X. et al. SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China. J Neurol 263, 2136–2138 (2016) doi:10.1007/s00415-016-8256-3

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Keywords

  • Intellectual Disability
  • Mental Impairment
  • White Matter Abnormality
  • Hereditary Spastic Paraplegia
  • Autosomal Recessive