Whole-exome sequencing identifies functional classes of gene mutations associated with bone marrow failure in pediatric Fanconi Anemia patients

TY - JOUR

T1 - Whole-exome sequencing identifies functional classes of gene mutations associated with bone marrow failure in pediatric Fanconi Anemia patients

AU - Wang, Shiyu

AU - Zbib, Natalia H.

AU - Skaist, Alyza

AU - Gui, Jiang

AU - Madero-Marroquin, Rafael

AU - De Marchi, Federico

AU - Gondek, Lukasz P.

AU - Matsui, William

AU - Lau, Bonnie W.

N1 - Funding Information: Shiyu Wang analyzed data, created figures, and wrote the paper. Natalia H. Zbib analyzed data and created figures. Jiang Gui provided statistical analysis. Alyza Skaist did the initial analysis of the whole-exome sequencing results. Rafael Madero-Marroquin and Federico De Marchi provided essential reagents and contributed to the research design. Lukasz P. Gondek contributed to the research design. William Matsui provided essential tools and contributed to the research design. Bonnie W. Lau designed the research study, performed the research, supervised analysis of the data, and helped write the paper. All named authors have fulfilled the criteria regarding contributions to this manuscript as described above, drafting the paper and revising it critically, and approve the submitted and final version. All authors report no conflict of interest. National Institutes of Health.

PY - 2021/8

Y1 - 2021/8

UR - http://www.scopus.com/inward/record.url?scp=85106208026&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85106208026&partnerID=8YFLogxK

U2 - 10.1111/ejh.13645

DO - 10.1111/ejh.13645

M3 - Letter

C2 - 33960532

AN - SCOPUS:85106208026

SN - 0902-4441

VL - 107

SP - 293

EP - 294

JO - European Journal of Haematology

JF - European Journal of Haematology

IS - 2

ER -