Showing 1 - 4 results of 4 for search 'Lettie E Rawlins', query time: 0.02s Refine Results
  1. 1
    Autophagy dysregulation via the USP20-ULK1 axis in the HERC2-related neurodevelopmental disorder

    Autophagy dysregulation via the USP20-ULK1 axis in the HERC2-related neurodevelopmental disorder by Joan Sala-Gaston, Eva M. Pérez-Villegas, José A. Armengol, Lettie E. Rawlins, Emma L. Baple, Andrew H. Crosby, Francesc Ventura, Jose Luis Rosa

    Published 2024-04-01
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  2. 2
    Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan

    Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan by Asif Naveed Ahmed, Lettie E. Rawlins, Niamat Khan, Zakir Jan, Nishanka Ubeyratna, Nikol Voutsina, Arfa Azeem, Saadullah Khan, Emma L. Baple, Andrew H. Crosby, Shamim Saleha

    Published 2024-10-01
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  3. 3
    Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families

    Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families by Arfa Azeem, Asif Naveed Ahmed, Niamat Khan, Nikol Voutsina, Irfan Ullah, Nishanka Ubeyratna, Muhammad Yasin, Emma L. Baple, Andrew H. Crosby, Lettie E. Rawlins, Shamim Saleha

    Published 2024-09-01
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  4. 4
    Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families

    Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families by Muhammad Marwan, Muhammad Dawood, Mukhtar Ullah, Irfan Ullah Shah, Niamat Khan, Muhammad Taimur Hassan, Muhammad Karam, Lettie E. Rawlins, Emma L Baple, Andrew H. Crosby, Shamim Saleha

    Published 2023-05-01
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