A 9-bp Deletion Homoplasmy in Women with Polycystic Ovary Syndrome Revealed by Mitochondrial Genome-Mutation Screen

Author： Zhuo Guangchao Feng Guofang Leng Jianhang Yu Lin Jiang Yan

ISSN： 0006-2928

Source： Biochemical Genetics, Vol.48, Iss.1-2, 2010-02, pp. : 157-163

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Mitochondrial DNA mutations may not be frequent in patients with polycystic ovary syndrome

By Chen Ruixiang Wang Huiling Li Shaoping Ren Yanfang

Mitochondrial DNA, Vol. 24, Iss. 4, 2013-08 ,pp. : 418-419

Informa Healthcare

Access to resources Recommend Favorite

Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion

By Montiel-Sosa Jose Francisco Herrero María Dolores

Mitochondrial DNA, Vol. 24, Iss. 4, 2013-08 ,pp. : 420-431

Informa Healthcare

Access to resources Recommend Favorite

Genetic variation in the vitamin D receptor gene and vitamin D serum levels in Egyptian women with polycystic ovary syndrome

By El-Shal Amal Shalaby Sally Aly Nader Rashad Nearmeen Abdelaziz Ahmed

Molecular Biology Reports, Vol. 40, Iss. 11, 2013-11 ,pp. : 6063-6073

Springer Publishing Company

Access to resources Recommend Favorite

Imbalanced circulating matrix metalloproteinases in polycystic ovary syndrome

By Gomes Valéria Vieira Carolina Jacob-Ferreira Anna Belo Vanessa Soares Gustavo Fernandes Janaína Ferriani Rui Tanus-Santos Jose

Molecular and Cellular Biochemistry, Vol. 353, Iss. 1-2, 2011-07 ,pp. : 251-257

Springer Publishing Company

Access to resources Recommend Favorite

Detection of the `4977 bp' mitochondrial DNA deletion in human atherosclerotic lesions

By Bogliolo Massimo

Mutagenesis, Vol. 14, Iss. 1, 1999-01 ,pp. : 77-82

Oxford University Press

Access to resources Recommend Favorite