Validation of a next-generation sequencing (NGS) panel to improve the diagnosis of X-linked hypophosphataemia (XLH) and other genetic disorders of renal phosphate wasting

Susanne Thiele, Ralf Werner, Annika Stubbe, Olaf Hiort*, Wolfgang Hoeppner

*Korrespondierende/r Autor/-in für diese Arbeit

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Biochemistry, Genetics and Molecular Biology

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