Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Mohammad Abanemai"'
Autor:
Nawal Makhseed, Majid Alfadhel, Hanan E. Shamseldin, Nisha Patel, Eissa Faqeih, Sateesh Maddirevula, Jumanah Alshenaifi, Dorota Monies, Majed Dasouki, Mais Hashem, Rifaat Rawashdeh, Wesam Kurdi, Adnan Hadid, Nour Ewida, Zuhair Rahbeeni, Eman Alobeid, Mohammed Zain Seidahmed, Amal Y. Kentab, Saeed Al Tala, Shams Anazi, Niema Ibrahim, Rawda Sunbul, Mohammed Al-Owain, Turki Alkharfi, Ranad Shaheen, Dia A. Mohammed, Mohammad Abanemai, Nada Al Tassan, Rana Alomar, Abdulrahman Alswaid, Fowzan S. Alkuraya, Heba Y. El Khashab, Salwa M. Alkhalifi, Saud H. AlDubayan, Wafaa Eyaid, Amal Alhashem, Suha Atyani, Mohamed Abouelhoda, Hamad Al-Zaidan, Firdous Abdulwahab, Minnie Jacob, Alya Qari, Zuhair N. Al-Hassnan, Nadia Alhashemi, Tarfa Al-Sheddi
Publikováno v:
Clinical genetics. 95(2)
Defects in the peroxisomes biogenesis and/or function result in peroxisomal disorders. In this study, we describe the largest Arab cohort to date (72 families) of clinically, biochemically and molecularly characterized patients with peroxisomal disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2d353841a8532bd0d1a86b9c7a1c1a6
https://pubmed.ncbi.nlm.nih.gov/30561787
https://pubmed.ncbi.nlm.nih.gov/30561787
