Homozygosity mapping reveals founderSEC23B-Y462C mutations in Indian congenital dyserythropoietic anemia type II-Reference-Cited by-同舟云学术

Homozygosity mapping reveals founderSEC23B-Y462C mutations in Indian congenital dyserythropoietic anemia type II

Author:

Singleton B.¹,Bansal D.²,Varma N.³,Das R.³,Naseem S.³,Saikia U.N.⁴,Malhotra P.⁵,Varma S.⁵,Marwaha R.K.²,King M.-J.⁶,Ahmed M.⁷^ORCID

Affiliation:

1. Bristol Institute for Transfusion Sciences; National Health Service Blood and Transplant (NHSBT); Bristol UK

2. Pediatric Haematology-Oncology Unit, Department of Paediatrics, Advanced Paediatrics Centre; PGIMER; Chandigarh India

3. Department of Haematology; PGIMER; Chandigarh India

4. Department of Histopathology; PGIMER; Chandigarh India

5. Department of Internal Medicine; PGIMER; Chandigarh India

6. Membrane Biochemistry; International Blood Group Reference Laboratory, NHSBT; Bristol UK

7. Department of Haematological Medicine, Leukaemia Genomics and Bone Marrow Failure Group; Kings College Hospital; London UK

Funder

Kings College London

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference8 articles.

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