A novel SLC4A1 mutation in a child with hereditary spherocytosis and distal renal tubular acidosis-Reference-Cited by-同舟云学术

A novel SLC4A1 mutation in a child with hereditary spherocytosis and distal renal tubular acidosis

Published:2022-04-20 Issue:11 Volume:69 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Giovanni Raimondo Pieri¹^ORCID,Ilaria Possenti¹,Andrea Secco¹,Pierangela Castorina²,Fabio Paglialonga³,Tommaso Mina⁴,Marco Zecca⁴^ORCID,Enrico Felici¹

Affiliation:

1. Pediatric and Pediatric Emergency Unit Children Hospital Alessandria Italy

2. Casa di Cura Igea Milan Italy

3. Pediatric Nephrology, Dialysis and Transplant Unit Fondazione Ca' Grande IRRCS Ospedale Maggiore Policlinico Milan Italy

4. Pediatric Hematology/Oncology Fondazione IRCCS Policlinico San Matteo Pavia Italy

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29729

Reference26 articles.

1. Hereditary spherocytosis

2. Distal renal tubular acidosis with hereditary spherocytosis

3. Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

4. Clinical and laboratory approaches in the diagnosis of renal tubular acidosis

5. Primary Autosomal Recessive Distal Renal Tubular Acidosis Caused by a Common HomozygousSLC4A1Mutation in Two Lao Families

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