The single nucleotide variant at c.662A>G in human RRM2B is a loss‐of‐function mutation-Reference-Cited by-同舟云学术

The single nucleotide variant at c.662A>G in human RRM2B is a loss‐of‐function mutation

Author:

Tseng Yen‐Tzu¹,Li Shang‐Wei²³,HuangFu Wei‐Chun²³,Yen Yun²³⁴⁵,Liu I‐Hsuan¹⁶⁷^ORCID

Affiliation:

1. Department of Animal Science and Technology National Taiwan University Taipei Taiwan

2. Graduate Institute of Cancer Biology and Drug Discovery College of Medical Science and Technology Taipei Medical University Taipei Taiwan

3. Ph.D. Program for Cancer Molecular Biology and Drug Discovery College of Medical Science and Technology Taipei Medical University Taipei Taiwan

4. TMU Research Center of Cancer Translational Medicine Taipei Medical University Taipei Taiwan

5. Cancer Center Taipei Municipal WanFang Hospital Taipei Taiwan

6. Research Center for Developmental Biology and Regenerative Medicine National Taiwan University Taipei Taiwan

7. School of Veterinary Medicine National Taiwan University Taipei Taiwan

Funder

Council of Agriculture

Ministry of Health and Welfare

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

Reference28 articles.

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