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pro vyhledávání: '"Batoul M, Baz"'
Autor:
Salma M, Wakil, Hatem N, Murad, Batoul M, Baz, Samiya T, Hagos, Rana A, Al-Amr, Suad A, Al-Yamani, Salem M, Al-Wadaee, Brian F, Meyer, Saeed A, Bohlega
Publikováno v:
Neurosciences (Riyadh, Saudi Arabia). 17(1)
To assess the mutational and clinical spectrum of spatacsin associated with autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC).A retrospective study was carried out at King Faisal Specialist Hospital and Researc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::027d05b016a7b87c2677f0228a2322a8
https://pubmed.ncbi.nlm.nih.gov/22246010
https://pubmed.ncbi.nlm.nih.gov/22246010
