Rh null phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population-Reference-Cited by-同舟云学术

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Rh null phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population

Published:2019-04-16 Issue:8 Volume:59 Page:2519-2522
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Ushiki Takashi¹^ORCID,Tsuneyama Hatsue²,Masuko Masayoshi³,Kozakai Takashi⁴,Kasami Takuya⁴,Tanaka Tomoyuki⁴,Uchikawa Makoto²,Kitajima Toshiki⁴,Kasai Emiko⁴,Komata Tae⁵,Katagiri Takayuki³,Kamimura Masami¹,Sato Kenji⁶,Fuse Ichiro⁵,Ogasawara Kenichi⁷,Nakata Koh¹

Affiliation:

1. Department of Transfusion Medicine, Cell Therapy and Regenerative Medicine Niigata University Medical and Dental Hospital Niigata Japan

2. Japanese Red Cross Kanto‐Koshinetsu Block Blood Center Tokyo Japan

3. Department of Hematology Niigata University Faculty of Medicine Niigata Japan

4. Department of Hematology Sado General Hospital Niigata Japan

5. Niigata Red Cross Blood Center Niigata Japan

6. Sado General Hospital Niigata Japan

7. Japanese Red Cross Central Blood Institute Tokyo Japan

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15312

Reference10 articles.

1. Hemolytic Anemia Associated with Rhnullbut not with Bombay Blood

2. Insights into the Structure and Function of Membrane Polypeptides Carrying Blood Group Antigens

3. Rh-null phenotype caused by a completeRHAGdeletion

4. A novel nucleotide deletion in RHAG allele identified in a Chinese Rhnull individual

5. A new Rhnullallele in francophone Quebecers

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