Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham)-Reference-Cited by-同舟云学术

Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham)

Published:2022-10-17 Issue:1 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Gorfinkel Lev¹^ORCID,Wachter Franziska¹^ORCID,Luo Hong‐yuan²,Hansbury Eileen¹,Williams David A.¹^ORCID,Agarwal Archana³,Chui David H. K.²,Cantor Alan B.¹⁴^ORCID

Affiliation:

1. Division of Pediatric Hematology‐Oncology Boston Children's Hospital/Dana‐Farber Cancer Institute Harvard Medical School Boston Massachusetts USA

2. Departments of Medicine Pathology and Laboratory Medicine Boston University School of Medicine Boston Massachusetts USA

3. Department of Pathology University of Utah Health Sciences Salt Lake City Utah USA

4. Harvard Stem Cell Institute Cambridge Massachusetts USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30067

Reference13 articles.

1. Hemoglobin Variants: Biochemical Properties and Clinical Correlates

2. Disorders of the synthesis of human fetal hemoglobin

3. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

4. A new unstable variant of the fetal hemoglobinHBG2gene: Hb F-Turritana [Gγ64(E8)Gly→Asp, HBG2:c.194G>A] foundin cisto the Hb F-Sardinia gene [Aγ(E19)Ile→Thr, HBG1:c.227T>C]

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