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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Familial glucocorticoid deficiency type 1 due to a novel compound heterozygous MC2R mutation

Artur Mazur1, Katrin Koehler, Markus Schuelke

  • 1Institute of Physiotherapy, University of Rzeszów, Poland.

Hormone Research
|May 28, 2008
PubMed
Abstract

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