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1991 | 1 |
1993 | 1 |
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A novel X-linked gene, G4.5. is responsible for Barth syndrome.
Nat Genet. 1996 Apr;12(4):385-9. doi: 10.1038/ng0496-385.
Nat Genet. 1996.
PMID: 8630491
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.
Bolhuis PA, Hensels GW, Hulsebos TJ, Baas F, Barth PG.
Bolhuis PA, et al.
Am J Hum Genet. 1991 Mar;48(3):481-5.
Am J Hum Genet. 1991.
PMID: 1998334
Free PMC article.
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Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.
Adès LC, Gedeon AK, Wilson MJ, Latham M, Partington MW, Mulley JC, Nelson J, Lui K, Sillence DO.
Adès LC, et al.
Am J Med Genet. 1993 Feb 1;45(3):327-34. doi: 10.1002/ajmg.1320450309.
Am J Med Genet. 1993.
PMID: 8434619
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