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A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report
Yahia, Ashraf
;
Chen, Zhefan Stephen
;
Ahmed, Ammar E.
;
Emad, Sara
;
Adil, Rawaa
;
Abubaker, Rayan
;
Taha, Shaimaa Omer M. A.
;
Salih, Mustafa A.
;
Elsayed, Liena
;
Chan, Ho Yin Edwin
;
Stevanin, Giovanni
(
BMC Neurology
,
2021
)
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Author
Abubaker, Rayan (1)
Adil, Rawaa (1)
Ahmed, Ammar E. (1)
Chan, Ho Yin Edwin (1)
Chen, Zhefan Stephen (1)
Elsayed, Liena (1)
Emad, Sara (1)
Salih, Mustafa A. (1)
Stevanin, Giovanni (1)
Taha, Shaimaa Omer M. A. (1)
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Subject
CCDC88C (1)
Hereditary spastic paraplegia (1)
Spinocerebellar ataxia type 40 (1)
Sudan (1)
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Date Issued
2021 (1)
Has File(s)
Yes (1)