Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset

Author:

Al‐Thihli Khalid12ORCID,Afting Cassian3,Al‐Hashmi Nadia4,Mohammed Mohammed4,Sliwinski Svenja3,Al Shibli Naema5,Al‐Said Khoula4,Al‐Kasbi Ghalia1,Al‐Kharusi Khalsa2,Merle Uta3,Füllekrug Joachim3ORCID,Al‐Maawali Almundher12ORCID

Affiliation:

1. Department of Genetics, College of Medicine and Health Sciences Sultan Qaboos University Muscat Oman

2. Genetic and Developmental Medicine Clinic Sultan Qaboos University Hospital Muscat Oman

3. Department of Internal Medicine IV Heidelberg University Hospital Heidelberg Germany

4. Department of Pediatrics and National Genetic Center Royal Hospital, Ministry of Health Muscat Oman

5. Department of Child Health, College of Medicine and Health Sciences Sultan Qaboos University Muscat Oman

Funder

Deutsche Forschungsgemeinschaft

Sultan Qaboos University

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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