المؤلفون: Ahangari, N, Gholampour-Faroji, N, Doosti, M, Ghayour Mobarhan, M, Shahrokhzadeh, S, Karimiani, EG, Hasani-Sabzevar, B, Torbati, PN, Haddad-Mashadrizeh, A

وصف الملف: application/pdf

Relation: https://openaccess.sgul.ac.uk/id/eprint/115313/1/Molec%20Gen%20Gen%20Med%20-%202023%20-%20Ahangari%20-%20ECEL1%20novel%20mutation%20in%20arthrogryposis%20type%205D%20A%20molecular%20dynamic%20simulation.pdf; Ahangari, N; Gholampour-Faroji, N; Doosti, M; Ghayour Mobarhan, M; Shahrokhzadeh, S; Karimiani, EG; Hasani-Sabzevar, B; Torbati, PN; Haddad-Mashadrizeh, A (2023) ECEL1 novel mutation in arthrogryposis type 5D: A molecular dynamic simulation study. Mol Genet Genomic Med, 11 (6). e2153. ISSN 2324-9269 https://doi.org/10.1002/mgg3.2153 SGUL Authors: Karimiani, Ehsan Ghayoor

الاتاحة: https://openaccess.sgul.ac.uk/id/eprint/115313/
https://openaccess.sgul.ac.uk/id/eprint/115313/1/Molec%20Gen%20Gen%20Med%20-%202023%20-%20Ahangari%20-%20ECEL1%20novel%20mutation%20in%20arthrogryposis%20type%205D%20A%20molecular%20dynamic%20simulation.pdf
https://doi.org/10.1002/mgg3.2153

المؤلفون: Vona B, Maroofian R, Bellacchio E, Najafi M, Thompson K, Alahmad A, He L, Ahangari N, Rad A, Shahrokhzadeh S, Bahena P, Mittag F, Traub F, Movaffagh J, Amiri N, Doosti M, Boostani R, Shirzadeh E, Haaf T, Diodato D, Schmidts M, Taylor RW, Karimiani EG

المصدر: BMC Medical Genetics, 12 November 2018

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/253155; https://eprints.ncl.ac.uk/fulltext.aspx?url=253155/00FD4CFE-6BEF-4892-90C8-1AEF8E51989B.pdf&pub_id=253155

الاتاحة: https://eprints.ncl.ac.uk/253155

المؤلفون: Vona, B, Maroofian, R, Bellacchio, E, Najafi, M, Thompson, K, Alahmad, A, He, L, Ahangari, N, Rad, A, Shahrokhzadeh, S, Bahena, P, Mittag, F, Traub, F, Movaffagh, J, Amiri, N, Doosti, M, Boostani, R, Shirzadeh, E, Haaf, T, Diodato, D, Schmidts, M, Taylor, RW, Karimiani, EG

وصف الملف: application/pdf

Relation: https://openaccess.sgul.ac.uk/id/eprint/110408/1/document.pdf; Vona, B; Maroofian, R; Bellacchio, E; Najafi, M; Thompson, K; Alahmad, A; He, L; Ahangari, N; Rad, A; Shahrokhzadeh, S; et al. Vona, B; Maroofian, R; Bellacchio, E; Najafi, M; Thompson, K; Alahmad, A; He, L; Ahangari, N; Rad, A; Shahrokhzadeh, S; Bahena, P; Mittag, F; Traub, F; Movaffagh, J; Amiri, N; Doosti, M; Boostani, R; Shirzadeh, E; Haaf, T; Diodato, D; Schmidts, M; Taylor, RW; Karimiani, EG (2018) Expanding the clinical phenotype of IARS2-related mitochondrial disease. BMC Med Genet, 19 (1). p. 196. ISSN 1471-2350 https://doi.org/10.1186/s12881-018-0709-3 SGUL Authors: Maroofian, Reza

الاتاحة: https://openaccess.sgul.ac.uk/id/eprint/110408/
https://openaccess.sgul.ac.uk/id/eprint/110408/1/document.pdf

المؤلفون: Vona B, Maroofian R, Bellacchio E, Najafi M, Thompson K, Alahmad A, He L, Ahangari N, Rad A, Shahrokhzadeh S, Bahena P, Mittag F, Traub F, Movaffagh J, Amiri N, Doosti M, Boostani R, Shirzadeh E, Haaf T, Diodato D, Schmidts M, Taylor RW, Karimiani EG

المصدر: BMC Medical Genetics, 12 November 2018

وصف الملف: application/pdf

الاتاحة: https://eprint.ncl.ac.uk/fulltext.aspx?url=253155/00FD4CFE-6BEF-4892-90C8-1AEF8E51989B.pdf&pub_id=253155