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Author/Creator Chapi, Marjan

1. A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Issue 1 (2nd January 2023)

Authors:
Daneshmandpour, Yousef; Bahmanpour, Zahra; Kazeminasab, Somayeh; Aghaei Moghadam, Ehsan; Alehabib, Elham; Chapi, Marjan; Tafakhori, Abbas; Aghaei, Negar; Darvish, Hossein; Emamalizadeh, Babak
Journal:
Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:
Volume 24:Issue 1/2(2023)
Page Start:
148
Record Type:
Journal Article
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2. COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. (11th July 2018)

Authors:
Suri, Fatemeh; Yazdani, Shahin; Chapi, Marjan; Safari, Iman; Rasooli, Paniz; Daftarian, Narsis; Jafarinasab, Mohammad Reza; Ghasemi Firouzabadi, Saghar; Alehabib, Elham; Darvish, Hossein; Klotzle, Brandy; Fan, Jian-Bing; Turk, Casey; Elahi, Elahe
Journal:
Human molecular genetics
Issue:
Volume 27:Number 21(2018:Nov. 01)
Page Start:
3772
Record Type:
Journal Article
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3. Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. (4th May 2019)

Authors:
Chapi, Marjan; Sabbaghi, Hamideh; Suri, Fatemeh; Alehabib, Elham; Rahimi-Aliabadi, Simin; Jamali, Faezeh; Jamshidi, Javad; Emamalizadeh, Babak; Darvish, Hossein; Mirrahimi, Mehraban; Ahmadieh, Hamid; Daftarian, Narsis
Journal:
Ophthalmic genetics
Issue:
Volume 40:Number 3(2019)
Page Start:
259
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗