Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran-Reference-Cited by-同舟云学术

Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran

Author:

Alimohammadi-Bidhendi Sara¹²,Azadmehr Sarah²³,Razipour Masoumeh²⁴,Zeinali Sirous²⁵,Eslami Maryam⁶⁷,Davoudi-Dehaghani Elham²

Affiliation:

1. Department of Genetics, Faculty of Advanced Technologies in Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran

2. Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran

3. Department of Genetics, Faculty of Basic Sciences, Shahr-e Rey, Payame Noor University, Tehran, Iran

4. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

5. Medical Genetics Laboratory of Dr. Zeinali, Kawsar Human Genetics Research Center, Tehran, Iran

6. Departments of Genetics, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran

7. Applied Biotechnology Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

Reference29 articles.

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