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Corrigendum: Caveolin-1 variant is associated with the metabolic syndrome in Kuwaiti children (Frontiers in Genetics ( 2018) 9 (689) DOI: 10.3389/fgene.2018.00689)

  • Rasheeba Nizam
  • , Ebaa Al-Ozairi
  • , Jo Max Goodson
  • , Motesam Melhem
  • , Lena Davidsson
  • , Hessa Alkhandari
  • , Ashraf Al Madhoun
  • , Sara Shamsah
  • , Malak Qaddoumi
  • , Ghazi Alghanim
  • , Nouf Alhasawi
  • , Mohamed Abu-Farha
  • , Jehad Abubaker
  • , Ping Shi
  • , Mor Li Hartman
  • , Mary Tavares
  • , Milad Bitar
  • , Hamad Ali
  • , Hossein Arefanian
  • , Sriraman Devarajan
  • Faisal Al-Refaei, Osama Alsmadi, Jaakko Tuomilehto, Fahd Al-Mulla

نتاج البحث

1 اقتباس (Scopus)

ملخص

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.

اللغة الأصليةEnglish
رقم المقال221
دوريةFrontiers in Genetics
مستوى الصوت10
رقم الإصدارMAR
المعرِّفات الرقمية للأشياء
حالة النشرPublished - 2019

Funding Agency

  • Kuwait Foundation for the Advancement of Sciences

بصمة

أدرس بدقة موضوعات البحث “Corrigendum: Caveolin-1 variant is associated with the metabolic syndrome in Kuwaiti children (Frontiers in Genetics ( 2018) 9 (689) DOI: 10.3389/fgene.2018.00689)'. فهما يشكلان معًا بصمة فريدة.

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