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Author/Creator Kenana, Rosan

3. ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder. Issue 3 (24th December 2014)

Authors:
Al-Hassnan, Zuhair N; Al-Dosary, Mazhor; Alfadhel, Majid; Faqeih, Eissa A; Alsagob, Maysoon; Kenana, Rosan; Almass, Rawan; Al-Harazi, Olfat S; Al-Hindi, Hindi; Malibari, Omhani I; Almutari, Faten B; Tulbah, Sahar; Alhadeq, Faten; Al-Sheddi, Tarfa; Alamro, Rana; AlAsmari, Ali; Almuntashri, Makki; ...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 3(2015)
Page Start:
186
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability. Issue 11 (31st August 2016)

Authors:
Kaya, Namik; Alsagob, Maysoon; D'Adamo, Maria Cristina; Al-Bakheet, Albandary; Hasan, Sonia; Muccioli, Maria; Almutairi, Faten B; Almass, Rawan; Aldosary, Mazhor; Monies, Dorota; Mustafa, Osama M; Alyounes, Banan; Kenana, Rosan; Al-Zahrani, Jawaher; Naim, Eva; Binhumaid, Faisal S; Qari, Alya; Alm...
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 11(2016)
Page Start:
786
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly. Issue 6 (25th March 2014)

Authors:
Faqeih, Eissa A.; Al‐Owain, Mohammed; Colak, Dilek; Kenana, Rosan; Al‐Yafee, Yusra; Al‐Dosary, Mazhor; Al‐Saman, Abdulaziz; Albalawi, Fadwa; Al‐Sarar, Dalia; Domiaty, Dalia; Daghestani, Maha; Kaya, Namik
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 6(2014.)
Page Start:
1565
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗