A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain-Reference-Cited by-同舟云学术

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A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain

Published:2005-03-01 Issue:5 Volume:105 Page:1946-1949
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:Blood

Author:

Callen E.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 82 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. FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia;Blood Advances;2024-02-15

2. Inherited Bone Marrow Failure Syndromes;Comprehensive Hematology and Stem Cell Research;2024

3. Fanconi Anemia;Reference Module in Biomedical Sciences;2024

4. Diagnóstico citogenético de AF en una cohorte de pacientes con características clínicas de sospecha de anemia de Fanconi;Pediatría;2023-06-28

5. Anemia de Fanconi, Parte 2. Estrategia metodológica para el diagnóstico molecular en pacientes con anemia de Fanconi;Acta Pediátrica de México;2023-02-14

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