The many faces of peroxisomal disorders: Lessons from a large Arab cohort Article

International Collaboration

cited authors

  • Alshenaifi, Jumanah; Ewida, Nour; Anazi, Shams; Shamseldin, Hanan E.; Patel, Nisha; Maddirevula, Sateesh; Al-Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Ibrahim, Niema; Hashem, Mais; Abdulwahab, Firdous; Jacob, Minnie; Alhashem, Amal; Alzaidan, Hamad I.; Seidahmed, Mohammed Z.; Alhashemi, Nadia; Rawashdeh, Rifaat; Eyaid, Wafaa; Al-Hassnan, Zuhair N.; Rahbeeni, Zuhair; Alswaid, Abdulrahman; Hadid, Adnan; Qari, Alya; Mohammed, Dia A.; El Khashab, Heba Y.; Alfadhel, Majid; Abanemai, Mohammad; Sunbul, Rawda; Al Tala, Saeed; Alkhalifi, Salwa; Alkharfi, Turki; Abouelhoda, Mohamed; Monies, Dorota; Al Tassan, Nada; AlDubayan, Saud H.; Kurdi, Wesam; Al-Owain, Mohammed; Dasouki, Majed J.; Kentab, Amal Y.; Atyani, Suha; Makhseed, Nawal; Faqeih, Eissa; Shaheen, Ranad; Alkuraya, Fowzan S.

authors

Publication Date

  • February 1, 2019

webpage

published in

category

keywords

  • VLCFA
  • Zellweger syndrome
  • founder mutation
  • genotype/phenotype correlation
  • peroxisomal disorder

start page

  • 310

end page

  • 319

volume

  • 95

issue

  • 2