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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 3
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Original Article

A New β0-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a Heterozygous P4.2 Nippon Gene

Chris AdhiyantoDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan;Faculty of Medicine and Health Science, Universitas Islam Negeri Syarif Hidayatullah, Jakarta, IndonesiaCorrespondence[email protected] [email protected]
,
Yasuhiro YamashiroDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Yukio HattoriDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Takenori NittaDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Minako HinoDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan
,
Maryam MatarDepartment of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan;United Arab Emirates Genetic Disease Association, Dubai, United Arab Emirates
,
Fumiya TakagiFukuyama Medical Center, Fukuyama, Japan
&
Masafumi KimotoFukuyama Medical Center, Fukuyama, Japan
 show all
Pages 227-240 | Received 19 Jul 2012, Accepted 10 Nov 2012, Published online: 22 Apr 2013

Citations (7)

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Read on this site (3)

Kun Yang, Quan Ren, Yi Wu, Yali Zhou & Xiaolin Yin. (2019) A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation. Hemoglobin 43:2, pages 140-144.
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Ferania Mella, Yasuhiro Yamashiro, Chris Adhiyanto, Tatehiko Tanaka, Takenori Nitta, Yuki Amao & Masafumi Kimoto. (2018) A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin. Hemoglobin 42:1, pages 1-6.
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Rakesh Kumar, Chandan Sagar, Dharmesh Sharma & Purnima Kishor. (2015) β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt. Hemoglobin 39:1, pages 1-8.
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Articles from other publishers (4)

Sri Anggarini Rasyid, Sanatang Sanatang, Satriani Syarif, Sugireng Sugireng, Titi Purnama, Suwarny Suwarny & Yayan Kurniansyah Saputra. (2021) Effect of Batissa violacea celebensis Martens, 1897, Extract on β-Catenin Gene in Mice (Mus musculus) Induced by Azoxymethane and Dextran Sulfate Sodium using Polymerase Chain Reaction-restriction Fragment Length Polymorphism Method. Open Access Macedonian Journal of Medical Sciences 9:A, pages 964-970.
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Soo Jin Kim, Jihyun Song, N. Scott Reading, Julio Lautersztain, Abdullah Kutlar, Archana M. Agarwal, Theresa L. Coetzer & Josef T. Prchal. (2021) Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations. American Journal of Hematology 96:5.
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Shuichi Otabe, Hitomi Nakayama, Tsuyoshi Ohki, Eri Soejima, Yuji Tajiri & Kentaro Yamada. (2016) Haemoglobin variants may cause significant differences in haemoglobin A1c as measured by high-performance liquid chromatography and enzymatic methods in diabetic patients: a cross-sectional study. Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 54:4, pages 432-437.
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Katsumi Iizuka, Masami Mizuno, Hiroyuki Niwa & Jun Takeda. (2015) A Rare Case of Variant Hemoglobin (Hb Yahata) Suspected Based on Inconsistent Plasma Glucose and HbA1c Levels. Internal Medicine 54:14, pages 1771-1775.
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