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A novel CLN2/TPP1 mutation in a patient with late infantile neuronal ceroid lipofuscinosis

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Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in this study involving human participant were in accordance with the ethical standards of the Affiliated Provincial Hospital of Anhui Medical University and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from the patient in the study.

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Author notes

    Authors and Affiliations

    1. Department of Neurology, The Affiliated Provincial Hospital of Anhui Medical University, No. 17, Lujiang Road, Hefei, 230022, China

      Feng Yu & Xiao-Min Liu

    2. Department of Orthopedic Surgery, The Affiliated Fuyang Hospital of Anhui Medical University, No. 17, Lujiang Road, Hefei, 230022, China

      Yin-He Chen

    3. Department of Biochemistry and Molecular Biology, Anhui Medical University, No. 81, Meishan Road, Hefei, 230022, China

      Sheng-Quan Zhang

    4. Department of Neurology, The First Affiliated Hospital of Anhui Medical University, No. 218, Jixi Road, Hefei, 230022, China

      Kai Wang

    Authors
    1. Feng Yu
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    2. Xiao-Min Liu
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    3. Yin-He Chen
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    4. Sheng-Quan Zhang
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    5. Kai Wang
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    Corresponding author

    Correspondence to Kai Wang.

    Additional information

    F. Yu and XM. Liu contributed equally to this work.

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    Yu, F., Liu, XM., Chen, YH. et al. A novel CLN2/TPP1 mutation in a patient with late infantile neuronal ceroid lipofuscinosis. Neurol Sci 36, 1917–1919 (2015). https://doi.org/10.1007/s10072-015-2272-4

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    • DOI: https://doi.org/10.1007/s10072-015-2272-4

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