Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD
Titel:
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD
Auteur:
Barclay, Sarah F. Rand, Casey M. Gray, Paul A. Gibson, William T. Wilson, Richard J.A. Berry-Kravis, Elizabeth M. Ize-Ludlow, Diego Bech-Hansen, N. Torben Weese-Mayer, Debra E.