Megaloblastic anemia and benign proteinuria: Clues to the diagnosis of Imerslund–Gräsbeck syndrome-Reference-Cited by-同舟云学术

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Megaloblastic anemia and benign proteinuria: Clues to the diagnosis of Imerslund–Gräsbeck syndrome

Published:2023-10-19 Issue:1 Volume:71 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Luo Xiaojuan¹,Wang Jieying²,Lin Zhenhu¹,Zhao Jiwei³,Cao Ke¹,Liu Jinlin⁴^ORCID

Affiliation:

1. Clinical Laboratory, Shenzhen Children's Hospital Shenzhen Guangdong China

2. Department of Laboratory Medicine The Second Affiliated Hospital of Hainan Medical University Haikou China

3. Department of Laboratory Medicine Nanjing Lishui District Hospital of Traditional Chinese Medicine Nanjing China

4. Department of Clinical Laboratory South China Hospital, Medical School Shenzhen University Shenzhen China

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30731

Reference5 articles.

1. Clinical and molecular characteristics of imerslund‐gräsbeck syndrome: First report of a novel Frameshift variant in Exon 11 of AMN gene

2. Immunodeficiency and inborn disorders of vitamin B12 and folate metabolism

3. National Center for Biotechnology Information. ClinVar; [VCV000056759.4] https://www.ncbi.nlm.nih.gov/clinvar/variation/VCV000056759.4(accessed2023).

4. Vitamin B12 absorption and malabsorption

5. A Patient with Cubilin Deficiency

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