1 |
Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis |
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| | Sarah Wiethoff,Georgia Xiromerisiou,Conceição Bettencourt,Anna Kioumi,Iakovos Tsiptsios,Athanasios Tychalas,Markousi Evaggelia,Kaltsounis George,Vasileios Makris,John Hardy,Henry Houlden | | | Journal of the Neurological Sciences. 2014; | | | [Pubmed] [Google Scholar] [DOI] | | 2 |
A novel XK gene mutation in a Taiwanese family with McLeod syndrome |
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| | Pei-Yun Chen,Szu-Chia Lai,Chih-Chao Yang,Ming-Jen Lee,Yen-Hui Chiu,Sui-Hing Yan,Chin-Song Lu,Tu-Hsueh Yeh | | | Journal of the Neurological Sciences. 2014; | | | [Pubmed] [Google Scholar] [DOI] | | 3 |
McLeod syndrome and acanthocytosis |
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| | Mehndiratta, M. | | | Annals of Indian Academy of Neurology. 2011; 14(2): 143 | | | [Pubmed] [Google Scholar] | | 4 |
McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity |
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| | Chakravarty, A., Bhattacharya, P., Banerjee, D., Mukherjee, S. | | | Annals of Indian Academy of Neurology. 2011; 14(2): 144 | | | [Pubmed] [Google Scholar] | |
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