TY - JOUR
T1 - Corrigendum
T2 - Caveolin-1 variant is associated with the metabolic syndrome in Kuwaiti children (Frontiers in Genetics ( 2018) 9 (689) DOI: 10.3389/fgene.2018.00689)
AU - Nizam, Rasheeba
AU - Al-Ozairi, Ebaa
AU - Goodson, Jo Max
AU - Melhem, Motesam
AU - Davidsson, Lena
AU - Alkhandari, Hessa
AU - Madhoun, Ashraf Al
AU - Shamsah, Sara
AU - Qaddoumi, Malak
AU - Alghanim, Ghazi
AU - Alhasawi, Nouf
AU - Abu-Farha, Mohamed
AU - Abubaker, Jehad
AU - Shi, Ping
AU - Hartman, Mor Li
AU - Tavares, Mary
AU - Bitar, Milad
AU - Ali, Hamad
AU - Arefanian, Hossein
AU - Devarajan, Sriraman
AU - Al-Refaei, Faisal
AU - Alsmadi, Osama
AU - Tuomilehto, Jaakko
AU - Al-Mulla, Fahd
N1 - Publisher Copyright:
Copyright © 2019 Nizam, Al-Ozairi, Goodson, Melhem, Davidsson, Alkhandari, Al Madhoun, Shamsah, Qaddoumi, Alghanim, Alhasawi, Abu-Farha, Abubaker, Shi, Hartman, Tavares, Bitar, Ali, Arefanian, Devarajan, Al-Refaei, Alsmadi, Tuomilehto and Al-Mulla.
PY - 2019
Y1 - 2019
N2 - Author names were incorrectly spelled as “Mark L. Hartman”, “Jihad Abubaker”, “Ebaa Alozairi”, and “Mohamed Abufarha”. The correct spelling is “Mor-Li Hartman”, “Jehad Abubaker”, “Ebaa Al-Ozairi”, and “Mohamed Abu-Farha”. The updated author contributions statement appears below. “RN and FA-M designed the study. FA-M, RN, and JG directed the work. OA, JG, SD, and M-LH directed study participant recruitment, sample processing, and data collection. FA-M, RN, HaA, and MB shortlisted the gene/variant. RN, MM, GA, and NA performed the experiment. FA-M, RN, and PS carried out statistical analysis and interpretation. EA-O, LD, HeA, MLH, MT, HoA, and FA-R carried out clinical data analysis and interpretation. RN and FA-M wrote the manuscript. EA-O, JT, LD, JG, AA, FA-R, SS, MQ, MA-F, JA, M-LH, PS, MB, HaA, and OA reviewed and edited the manuscript. FA-M, EA-O, and JT critically revised and approved the manuscript.” The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
AB - Author names were incorrectly spelled as “Mark L. Hartman”, “Jihad Abubaker”, “Ebaa Alozairi”, and “Mohamed Abufarha”. The correct spelling is “Mor-Li Hartman”, “Jehad Abubaker”, “Ebaa Al-Ozairi”, and “Mohamed Abu-Farha”. The updated author contributions statement appears below. “RN and FA-M designed the study. FA-M, RN, and JG directed the work. OA, JG, SD, and M-LH directed study participant recruitment, sample processing, and data collection. FA-M, RN, HaA, and MB shortlisted the gene/variant. RN, MM, GA, and NA performed the experiment. FA-M, RN, and PS carried out statistical analysis and interpretation. EA-O, LD, HeA, MLH, MT, HoA, and FA-R carried out clinical data analysis and interpretation. RN and FA-M wrote the manuscript. EA-O, JT, LD, JG, AA, FA-R, SS, MQ, MA-F, JA, M-LH, PS, MB, HaA, and OA reviewed and edited the manuscript. FA-M, EA-O, and JT critically revised and approved the manuscript.” The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
UR - http://www.scopus.com/inward/record.url?scp=85066601354&partnerID=8YFLogxK
U2 - 10.3389/fgene.2019.00221
DO - 10.3389/fgene.2019.00221
M3 - Comment/debate
AN - SCOPUS:85066601354
SN - 1664-8021
VL - 10
JO - Frontiers in Genetics
JF - Frontiers in Genetics
IS - MAR
M1 - 221
ER -