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Saber, Siamak
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1

Allelic Dropout Is a Common Phenomenon That Reduces the Dia..:

Shestak, Anna G. ; Bukaeva, Anna A. ; Saber, Siamak.
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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2

A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic..:

Sadeghi, Zahra ; Chavoshi Tarzjani, Seyedeh Parisa ; Miri Moosavi, Reyhaneh Sadat..
International Medical Case Reports Journal.  13 (2020)  - p. 291-296 , 2020
Link: https://doi.org/10.2147/..
 
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3

Mutational Spectrum of the SCN5A gene in Brugada Syndrome P..:

Shestak, Anna ; Saber, Siamak ; Makarov, Leonid.
Journal of Electrocardiology.  53 (2019)  - p. e5-e6 , 2019
Link: https://doi.org/10.1016/..
 
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4

Mutational Spectrum of the SCN5A gene in Brugada Syndrome P..:

Shestak, Anna ; Saber, Siamak ; Makarov, Leonid.
Journal of Electrocardiology.  51 (2018)  6 - p. 1166 , 2018
Link: https://doi.org/10.1016/..
 
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5

Detection of a new KCNQ1 frameshift mutation associated wit..:

Amirian, Azam ; Zafari, Zahra ; Dalili, Mohammad...
Journal of Arrhythmia.  34 (2018)  3 - p. 286-290 , 2018
Link: https://doi.org/10.1002/..
 
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6

Identification and characterization of a novel recessive KC..:

Zafari, Zahra ; Dalili, Mohammad ; Zeinali, Sirus...
Journal of Electrocardiology.  50 (2017)  6 - p. 912-918 , 2017
Link: https://doi.org/10.1016/..
 
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7

Identification of a new mutation in an Iranian family with ..:

Akbaroghli, Susan ; Balali, Maryam ; Kamalidehghan, Behnam...
Therapeutics and Clinical Risk Management.  13 (2016)  - p. 15-19 , 2016
Link: https://doi.org/10.2147/..
 
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8

Complex genetic background in a large family with Brugada s..:

Saber, Siamak ; Amarouch, Mohamed-Yassine ; Fazelifar, Amir-Farjam...
Physiological Reports.  3 (2015)  1 - p. e12256 , 2015
Link: https://doi.org/10.14814..
 
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9

Positive Brugada Challenge Test in V1R–V3R as a Predictor o..:

Hashemi, Arash ; Shahrzad, Shahab ; Shahrzad, Sorayya...
Annals of Noninvasive Electrocardiology.  18 (2013)  5 - p. 421-426 , 2013
Link: https://doi.org/10.1111/..
 
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10

Sodium Current and Potassium Transient Outward Current Gene..:

Holst, Anders G. ; Saber, Siamak ; Houshmand, Massoud...
Canadian Journal of Cardiology.  28 (2012)  2 - p. 196-200 , 2012
Link: https://doi.org/10.1016/..
 
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11

Accumulation of mitochondrial genome variations in Persian ..:

Khatami, Mehri ; Houshmand, Massoud ; Sadeghizadeh, Majid...
Cardiovascular Pathology.  19 (2010)  2 - p. e21-e27 , 2010
Link: https://doi.org/10.1016/..
 
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12

A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic..:

Sadeghi, Zahra ; Chavoshi Tarzjani, Seyedeh Parisa ; Miri Moosavi, Reyhaneh Sadat..
info:eu-repo/semantics/altIdentifier/doi/10.2147/IMCRJ.S257654.  , 2020
Link: https://www.dovepress.co..
 
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13

Identification of a new mutation in an Iranian family with ..:

Akbaroghli, Susan ; Balali, Maryam ; Kamalidehghan, Behnam...
info:eu-repo/semantics/altIdentifier/doi/10.2147/TCRM.S111717.  , 2016
Link: https://www.dovepress.co..
 
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14

Complex genetic background in a large family with Brugada s..:

Saber, Siamak ; Amarouch, Mohamed Yassine ; Fazelifar, Amir-Farjam...
https://boris.unibe.ch/80625/.  , 2015
Link: https://boris.unibe.ch/8..
 
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15

Table_2_Allelic Dropout Is a Common Phenomenon That Reduces..:

Anna G. Shestak ; Anna A. Bukaeva ; Siamak Saber.
doi:10.3389/fgene.2021.620337.s003.  , 2021
Link: https://doi.org/10.3389/..
 
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