A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India

Published:2021-03 Issue: Volume:Volume 14 Page:77-85
ISSN:1178-704X
Container-title:The Application of Clinical Genetics
language:en
Short-container-title:TACG

Author:

Chauhan Waseem^ORCID,Afzal Mohammad,Zaka-ur-Rab Zeeba,Noorani Md Salik

Publisher

Informa UK Limited

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Global Epidemiology of Hemoglobin Disorders

2. Epidemiology of haemoglobin disorders in Europe: an overview

3. Newborn screening for hemoglobinopathies in California

4. Cooley’s anæmia (erythroblastic or mediterranean anæmia)

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of novel mutations in β-thalassemia patients in Maysan Governorate, Iraq;Molecular Biology Reports;2023-01-22

2. Direct sequencing of β-globin gene reveals a rare combination of two exonic and two intronic variants in a β-thalassemia major patient: a case report;Journal of Medical Case Reports;2022-10-09

3. First Report of the 3'-Untranslated Region +1506 (A>C) [NM_000518.5: c.*32A>C] mutation on the β-Globin Gene in the Indian Population;Hemoglobin;2021-12-09

4. IVS-II-16 (G>C) (HBB: c.315+16G>C) or IVS-II-666 (C>T) (HBB: c.316-185C>T) Mutations Trigger an Hb S (HBB: c.20A>T)/β+-Thalassemia Phenotype in an Hb S Trait Patient;Hemoglobin;2021-07-04

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP