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Author/Creator Mohammed, Inaam N.

1. A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal‐Recessive Juvenile‐Onset Parkinson's Disease. Issue 2 (19th January 2016)

Authors:
Elsayed, Liena Elbaghir Omer; Drouet, Valérie; Usenko, Tatiana; Mohammed, Inaam N.; Hamed, Ahlam AbdAlrahman Ahmed; Elseed, Maha Abdelmoneim; Salih, Mustafa A.M.; Koko, Mahmoud Eltayeb; Mohamed, Ashraf Yahia Osman; Siddig, Rayan Abubaker; Elbashir, Mustafa Idris; Ibrahim, Muntaser Eltayeb; Durr, ...
Journal:
Annals of neurology
Issue:
Volume 79:Issue 2(2016:Feb.)
Page Start:
335
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families. (10th June 2021)

Authors:
Koko, Mahmoud; Yahia, Ashraf; Elsayed, Liena E.; Hamed, Ahlam A.; Mohammed, Inaam N.; Elseed, Maha A.; Hamad, Muddathir H. A.; Babai, Arwa M.; Siddig, Rayan A.; Abd Allah, Amal S. I.; Mohamed, Mayada; EL‐Amin, Melka; Esteves, Typhaine; Altmüller, Janine; Toliat, Mohammad Reza; Thiele, Holger; Nür...
Journal:
Annals of human genetics
Issue:
Volume 85:Number 5(2021)
Page Start:
186
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing. (3rd February 2022)

Authors:
Yahia, Ashraf; Ayed, Ikhlas Ben; Hamed, Ahlam A.; Mohammed, Inaam N.; Elseed, Maha A.; Bakhiet, Aisha M.; Guillot‐Noel, Lena; Abozar, Fatima; Adil, Rawaa; Emad, Sara; Abubaker, Rayan; Musallam, Mhammed Alhassan; Eltazi, Isra Z. M.; Omer, Zulfa; Maaroof, Omer M.; Soussi, Amal; Bouzid, Amal; Kmiha,...
Journal:
Annals of human genetics
Issue:
Volume 86:Number 4(2022)
Page Start:
181
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗