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A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population.

Zahra Sadr, Davood Zare-Abdollahi, Mohammad Rohani, Afagh Alavi

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2023 Jul


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    No abstract available.

    Citation

    Zahra Sadr, Davood Zare-Abdollahi, Mohammad Rohani, Afagh Alavi. A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2023 Jul;44(7):2599-2602

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    PMID: 36854932

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