دورية أكاديمية
Rhnull phenotype: A family study of a novel RHAG allele in Brazilians.
| العنوان: | Rhnull phenotype: A family study of a novel RHAG allele in Brazilians. |
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| المؤلفون: | de Paula Vendrame TA; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Silva FS; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Silva NM; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Satake M; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Cortez APJ; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Castilho L; Hemocentro - Unicamp, Campinas, Brazil., Latini FRM; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil., Arnoni CP; Colsan - Associação Beneficente de Coleta de Sangue, São Paulo, Brazil. |
| المصدر: | Transfusion [Transfusion] 2022 Nov; Vol. 62 (11), pp. E66-E67. Date of Electronic Publication: 2022 Sep 12. |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-2995 (Electronic) Linking ISSN: 00411132 NLM ISO Abbreviation: Transfusion Subsets: MEDLINE |
| أسماء مطبوعة: | Original Publication: Arlington, Va. : American Association Of Blood Banks |
| مواضيع طبية MeSH: | Rh-Hr Blood-Group System*/genetics , Blood Proteins*/genetics, Alleles ; Brazil ; Phenotype |
| References: | Daniels GL. Human blood groups. Third ed. Wiley-Blackwell: Oxford, UK; 2013. Huang CH. Molecular insights into the Rh protein family and associated antigens. Curr Opin Hematol. 1997;4:94-103. Cartron JP. RH blood group system and molecular basis of Rh-deficiency. Baillieres Best Pract Res Clin Haematol. 1999;12:655-89. Fichou Y, Le Marechal C, Bryckaert L, Dupont I, Jamet D, Chen JM, et al. A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes. Transfusion. 2013;53:2974-82. Tian L, Song N, Yao ZQ, Huang M, Hou L. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene. Transfusion. 2011;51:2686-9. |
| فهرسة مساهمة: | Keywords: blood group genomics; immunohematology; molecular biology |
| المشرفين على المادة: | 0 (Rh-Hr Blood-Group System) 0 (Blood Proteins) |
| تواريخ الأحداث: | Date Created: 20220912 Date Completed: 20221109 Latest Revision: 20221201 |
| رمز التحديث: | 20221213 |
| DOI: | 10.1111/trf.17102 |
| PMID: | 36093570 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1537-2995 |
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| DOI: | 10.1111/trf.17102 |