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Dive into the research topics of 'Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD'. Together they form a unique fingerprint.- Sort by
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Sarah F. Barclay*, Casey M. Rand, Paul A. Gray, William T. Gibson, Richard J.A. Wilson, Elizabeth M. Berry-Kravis, Diego Ize-Ludlow, N. Torben Bech-Hansen, Debra E. Weese-Mayer
Research output: Contribution to journal › Article › peer-review