TY - JOUR
T1 - Erratum
T2 - Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies (Orphanet Journal of Rare Diseases (2020) 15: 126 DOI: 10.1186/s13023-020-01379-8)
AU - Opladen, Thomas
AU - López-Laso, Eduardo
AU - Cortès-Saladelafont, Elisenda
AU - Pearson, Toni S.
AU - Sivri, H. Serap
AU - Yildiz, Yilmaz
AU - Assmann, Birgit
AU - Kurian, Manju A.
AU - Leuzzi, Vincenzo
AU - Heales, Simon
AU - Pope, Simon
AU - Porta, Francesco
AU - García-Cazorla, Angeles
AU - Honzík, Tomáš
AU - Pons, Roser
AU - Regal, Luc
AU - Goez, Helly
AU - Artuch, Rafael
AU - Hoffmann, Georg F.
AU - Horvath, Gabriella
AU - Thöny, Beat
AU - Scholl-Bürgi, Sabine
AU - Burlina, Alberto
AU - Verbeek, Marcel M.
AU - Mastrangelo, Mario
AU - Friedman, Jennifer
AU - Wassenberg, Tessa
AU - Jeltsch, Kathrin
AU - Kulhánek, Jan
AU - Kuseyri Hübschmann, Oya
N1 - Publisher Copyright:
© 2020 The Author(s). Reference.
PY - 2020/8/5
Y1 - 2020/8/5
N2 - Following the original article's publication [1] the authors asked for the correction of Fig. 2, since the names of the disease genes [GCH1 and PCBD1] in the figure published did not match the listed diseases [AR-GTPCHD and PCDD]. The correct Fig. 2 isshown below: In the context of the manuscript correction and inorder to match he text content, the words "apart from DHPRD" should be removed from the second row and second column of Table 4, as shown below: (Table Presented).
AB - Following the original article's publication [1] the authors asked for the correction of Fig. 2, since the names of the disease genes [GCH1 and PCBD1] in the figure published did not match the listed diseases [AR-GTPCHD and PCDD]. The correct Fig. 2 isshown below: In the context of the manuscript correction and inorder to match he text content, the words "apart from DHPRD" should be removed from the second row and second column of Table 4, as shown below: (Table Presented).
UR - http://www.scopus.com/inward/record.url?scp=85089171611&partnerID=8YFLogxK
U2 - 10.1186/s13023-020-01464-y
DO - 10.1186/s13023-020-01464-y
M3 - Comment/debate
C2 - 32758270
AN - SCOPUS:85089171611
SN - 1750-1172
VL - 15
JO - Orphanet Journal of Rare Diseases
JF - Orphanet Journal of Rare Diseases
IS - 1
M1 - 202
ER -