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MeSH:(Oxidoreductases Acting on Sulfur Group Donors/genetics/*metabolism)

1.Analysis of SUOX gene variants and clinical features in a child with Isolated sulfite oxidase deficiency.

Yujuan WANG ; Xinqiang LAN

Chinese Journal of Medical Genetics 2023;40(2):177-180

2.Analysis of ETFDH gene variation in a Chinese family affected with lipid storage myopathy.

Yanjie XIA ; Xiangdong KONG

Chinese Journal of Medical Genetics 2019;36(10):1002-1005

3.Mutation analysis for a family affected with riboflavin responsive-multiple acyl-CoA dehydrogenase deficiency.

Jun LU ; Lijuan JI

Chinese Journal of Medical Genetics 2014;31(4):428-432

4.Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Dao-Jun HONG ; Min ZHU ; Zi-Juan ZHU ; Lu CONG ; Shan-Shan ZHONG ; Ling LIU ; Jun ZHANG

Chinese Medical Journal 2019;132(3):275-284

5.Nuclear factor E2-related factor 2 Dependent Overexpression of Sulfiredoxin and Peroxiredoxin III in Human Lung Cancer.

Young Sun KIM ; Hye Lim LEE ; Ki Bum LEE ; Joo Hun PARK ; Wou Young CHUNG ; Keu Sung LEE ; Seung Soo SHEEN ; Kwang Joo PARK ; Sung Chul HWANG

The Korean Journal of Internal Medicine 2011;26(3):304-313

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