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).

Erratum: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies / Opladen, T.; Lopez-Laso, E.; Cortes-Saladelafont, E.; Pearson, T. S.; Sivri, H. S.; Yildiz, Y.; Assmann, B.; Kurian, M. A.; Leuzzi, V.; Heales, S.; Pope, S.; Porta, F.; Garcia-Cazorla, A.; Honzik, T.; Pons, R.; Regal, L.; Goez, H.; Artuch, R.; Hoffmann, G. F.; Horvath, G.; Thony, B.; Scholl-Burgi, S.; Burlina, A.; Verbeek, M. M.; Mastrangelo, M.; Friedman, J.; Wassenberg, T.; Jeltsch, K.; Kulhanek, J.; Kuseyri Hubschmann, O.. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 15:1(2020). [10.1186/s13023-020-01464-y]

Erratum: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies

Leuzzi V.;Mastrangelo M.;
2020

Abstract

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).
2020
Tetrahydrobiopterin deficiency; BH4; Neurotransmitter; Guanosine triphosphate cyclohydrolase deficiency
01 Pubblicazione su rivista::01b Commento, Erratum, Replica e simili
Erratum: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies / Opladen, T.; Lopez-Laso, E.; Cortes-Saladelafont, E.; Pearson, T. S.; Sivri, H. S.; Yildiz, Y.; Assmann, B.; Kurian, M. A.; Leuzzi, V.; Heales, S.; Pope, S.; Porta, F.; Garcia-Cazorla, A.; Honzik, T.; Pons, R.; Regal, L.; Goez, H.; Artuch, R.; Hoffmann, G. F.; Horvath, G.; Thony, B.; Scholl-Burgi, S.; Burlina, A.; Verbeek, M. M.; Mastrangelo, M.; Friedman, J.; Wassenberg, T.; Jeltsch, K.; Kulhanek, J.; Kuseyri Hubschmann, O.. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 15:1(2020). [10.1186/s13023-020-01464-y]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1471035
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