Familial dilated cardiomyopathy and human leucocyte antigen. A report of two family cases.:A Report of Two Family Cases
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概要
- 論文の詳細を見る
Two familial cases of dilated cardiomyopathy were evaluated by HL-A typing. In the case of the first family, the mode of inheritance is likely to be an autosomal dominant trait. Only the affected individuals carried the identical HL-A haplotype (A2, Bw54, Cwl, DR4, DQw3), while the unaffected members do not share this pattern. In the second family case, the disease is probably inherited by autosomal recessive traits. All of the family members examined shared the identical HL-A haplotype (A24, Bw52, DR2, DQw1), but only the affected individuals were homozygous for this haplotype.
- International Heart Journal刊行会の論文
著者
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Ota Masao
Department Of Legal Medicine Shinshu University School Of Medicine
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Koike Seiichi
Second Department of Internal Medicine, Shinshu University school of Medicine
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Furuta Seiichi
Second Department of Internal Medicine, Shinshu University school of Medicine
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Kawa Shigeyuki
Second Department Of Internal Medicine Shinshu University Medical School
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Sasaki Yasuyuki
Second Department Of Internal Medicine Shinshu University School Of Medicine
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YABU Kouji
Second Department of Internal Medicine, Shinshu University School of Medicine
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ENDO Ryohei
Second Department of Internal Medicine, Shinshu University School of Medicine
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