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Neu-laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the l-serine biosynthesis pathway
Rocio Acuna-Hidalgo, Denny Schanze, Ariana Kariminejad, Ann Nordgren, Mohamad Hasan Kariminejad, Peter Conner, Giedre Grigelioniene, Daniel Nilsson, Magnus Nordenskjold, Anna Wedell, Christoph Freyer, Anna Wredenberg, Dagmar Wieczorek, Gabriele Gillessen-Kaesbach, Hulya Kayserili, Nursel Elcioglu, Siavash Ghaderi-Sohi, Payman Goodarzi, Hamidreza Setayesh, Maartje Van De Vorst
*Corresponding author for this work
- Radboud University Nijmegen
- Institute of Human Genetics
- Otto von Guericke University Magdeburg
- Kariminejad-Najmabadi Pathology and Genetics Center
- Cardiothoracic Surgery Unit
- Karolinska Institutet
- Department of Clinical Genetics
- Center for Fetal Medicine
- Centre for Inherited Metabolic Diseases
- Department of Laboratory Medicine
- Institut fur Humangenetik
- University of Duisburg-Essen
- Department of Medical Genetics
- Istanbul University
- Pediatrics Genetics Division
- Marmara University
- University of Innsbruck
- Department of Pediatrics
- University of California San Francisco
- University of Ottawa
25
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(Scopus)