Bernard–Soulier syndrome caused by two novel heterozygous GP1BA gene mutations: a case report and literature review

Senlin Zhanga Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Jing Linga Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Kai Cuia Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Shihong Zhanb Department of Neonatology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Jiajia Zhenga Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Wenyi Wanga Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaView further author information

Junjie Fana Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaCorrespondence[email protected]
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Shaoyan Hua Department of Hematology and Oncology, Children’s Hospital of Soochow University, Suzhou, People’s Republic of ChinaCorrespondence[email protected]
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Bernard–Soulier syndrome caused by two novel heterozygous GP1BA gene mutations: a case report and literature review

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Bernard–Soulier syndrome caused by two novel heterozygous GP1BA gene mutations: a case report and literature review

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