Role of heteroplasmic mutations in the mitochondrial genome and the ID4 gene promoter methylation region in the pathogenesis of chronic aplastic anemia in patients suffering from Kidney yin deficiency-Reference-Cited by-同舟云学术

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Role of heteroplasmic mutations in the mitochondrial genome and the ID4 gene promoter methylation region in the pathogenesis of chronic aplastic anemia in patients suffering from Kidney yin deficiency

Published:2015-04-29 Issue:6 Volume:22 Page:412-419
ISSN:1672-0415
Container-title:Chinese Journal of Integrative Medicine
language:en
Short-container-title:Chin. J. Integr. Med.

Author:

Cui Xing,Wang Jing-yi,Liu Kui,Cui Si-yuan,Zhang Jie,Luo Ya-qin,Wang Xin

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Complementary and alternative medicine,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11655-014-1813-7.pdf

Reference15 articles.

1. DiMauro S, Schon EA. Mitochondrial respiratory-chain diseases. N Engl J Med 2003;348:2656–2668.

2. Shadel GS, Clayton DA. Mitochondrial DNA maintenance in vertebrates. Annu Rev Biochem 1997;66:409–435.

3. Chinnery P, Schon E. Mitochondria. J Neurol Neurosurg Psychiatry 2003;74:1188–1199.

4. Giles RE, Blanc H, Cann HM, Wallace DC. Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci USA 1980;77:6715–6719.

5. Zhang ZN, Shen T, eds. Standard of diagnosis and treatment of hematology. 3rd ed. Beijing: Science Press; 2007:20.

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