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Establishing a core outcome set for creatine transporter deficiency and guanidinoacetate methyltransferase deficiency

Title:	Establishing a core outcome set for creatine transporter deficiency and guanidinoacetate methyltransferase deficiency
Authors:	Nasseri Moghaddam, Zahra^Aff1; Reinhardt, Emily K.^{Aff2, IDs13023025039003_cor1}; Thurm, Audrey^Aff3; Potter, Beth K.^Aff4; Smith, Maureen^Aff5; Graham, Celeste^{Aff2, Aff6}; Tiller, Beth H.^Aff6; Baker, Steven A.^Aff7; Bilder, Deborah A.^Aff8; Bogar, Regina^Aff6; Britz, Jacobus^Aff6; Cafferty, Rachel^Aff6; Coller, Daniel P.^{Aff2, Aff6}; DeGrauw, Ton J.^Aff9; Hall, Vicky^Aff6; Lipshutz, Gerald S.^Aff10; Longo, Nicola^{Aff9, Aff10}; Mercimek-Andrews, Saadet^{Aff9, Aff11}; Miller, Judith S.^Aff12; Pasquali, Marzia^{Aff9, Aff13}; Salomons, Gajja S.^{Aff9, Aff14}; Schulze, Andreas^{Aff9, Aff15}; Wheaton, Celine P.^Aff6; Williams, Kayla F.^Aff6; Young, Sarah P.^{Aff9, Aff16}; Li, Jasmine^Aff1; Balog, Sofia^{Aff2, Aff19}; Selucky, Theresa^Aff17; Stöckler-Ipsiroglu, Sylvia^{Aff1, Aff9, Aff18}; Wallis, Heidi^{Aff2, Aff6}
Source:	Orphanet Journal of Rare Diseases. 20(1)
Database:	Springer Nature Journals