Fructose 1,6‐bisphosphatase deficiency as a cause of childhood interstitial lung disease-Reference-Cited by-同舟云学术

Fructose 1,6‐bisphosphatase deficiency as a cause of childhood interstitial lung disease

Author:

Devaney Rebecca¹,Simpson Timothy²,Bush Andrew³^ORCID,Jagani Sumit⁴,Nicholson Andrew G.⁵,Semple Thomas⁶,Bhatt Jayesh Mahendra⁷^ORCID

Affiliation:

1. ST8 Paediatric Respiratory Medicine, Nottingham Children's Hospital Nottingham University Hospitals NHS Trust Nottingham UK

2. Faculty of Medicine & Health Sciences University of Nottingham Nottingham UK

3. Imperial College, Consultant Paediatric Chest Physician, Royal Brompton & Harefield NHS Foundation Trust, NIHR Senior Investigator Emeritus UK

4. Nottingham University Hospitals NHS Trust

5. Department of Histopathology Royal Brompton and Harefield NHS Foundation Trust and National Heart and Lung Institute, Imperial College London UK

6. Royal Brompton And Harefield Hospitals NHS Foundation Trust, Royal Brompton Hospital London UK

7. Paediatric Respiratory Medicine, Nottingham Children's Hospital Nottingham University Hospitals NHS Trust, Queen's Medical Centre Nottingham UK

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

Reference8 articles.

1. Fructose‐1 6‐Bisphosphatase 1; FBP1[Internet]. Available from:https://omim.org/entry/611570

4. Early onset children's interstitial lung diseases: discrete entities or manifestations of pulmonary dysmaturity?;Bush A;Paediatr Respir Rev,2018

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