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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 24, 2013 - Issue 5
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Full Length Research Paper

T4216C mutation in NADH dehydrogenase I gene is associated with recurrent pregnancy loss

Abasalt Hosseinzadeh Colagar
,
Elaheh MosaiebyDepartment of Molecular and Cell Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar Postal Code 47416-95447 Mazandaran, Iran
,
Seyed Mohammad SeyedhassaniResearch and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
,
Maryam MohajeraniDepartment of Molecular and Cell Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar Postal Code 47416-95447 Mazandaran, Iran
,
Ahoora ArastehDepartment of Medical Genetics, Special Medical Center, Tehran, Iran
,
Behnam KamalidehghanDepartment of Pharmacy, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
&
Massoud HoushmandCorrespondence[email protected]
 show all
Pages 610-612 | Received 16 Dec 2012, Accepted 29 Jan 2013, Published online: 06 Mar 2013

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Zhaochang Jiang, Lili Teng, Shunrong Zhang & Yu Ding. (2021) Mitochondrial ND1 T4216C and ND2 C5178A mutations are associated with maternally transmitted diabetes mellitus. Mitochondrial DNA Part A 32:2, pages 59-65.
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Ali Azadi, Dong Joo Seo, Hannaneh Jafari Sasansara & Michael Van Haute. (2018) Mitochondrial DNA variations are associated with recurrent pregnancy loss. Mitochondrial DNA Part A 29:5, pages 674-678.
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Maryam Balali, Behnam Kamalidehghan, Mohammad Farhadi, Fatemeh Ahmadipour, Mahmoud Dehghani Ashkezari, Mohsen Rezaei Hemami, Hossein Arabzadeh, Masoumeh Falah, Goh Yong Meng & Massoud Houshmand. (2016) Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss. Therapeutics and Clinical Risk Management 12, pages 117-128.
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Articles from other publishers (8)

Belén Monge-Ochoa, Luis Montoro, Julio Montoya, Eduardo Ruiz-Pesini, Manuel J. López-Pérez, Francisco de Castro & Carmen Díez-Sánchez. (2023) m.4216 T > C polymorphism in JT cluster determines a lower pregnancy rate in response to controlled ovarian stimulation treatment. Journal of Assisted Reproduction and Genetics 40:3, pages 671-682.
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Olga Aleksandrovna Solovova & Vyacheslav Borisovich Chernykh. (2022) Genetics of Oocyte Maturation Defects and Early Embryo Development Arrest. Genes 13:11, pages 1920.
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Whitney Cowell, Kelly Brunst, Elena Colicino, Li Zhang, Xiang Zhang, Tessa R. Bloomquist, Andrea A. Baccarelli & Rosalind J. Wright. (2021) Placental mitochondrial DNA mutational load and perinatal outcomes: Findings from a multi-ethnic pregnancy cohort. Mitochondrion 59, pages 267-275.
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Hong Ma, Tomonari Hayama, Crystal Van Dyken, Hayley Darby, Amy Koski, Yeonmi Lee, Nuria Marti Gutierrez, Satsuki Yamada, Ying Li, Michael Andrews, Riffat Ahmed, Dan Liang, Thanasup Gonmanee, Eunju Kang, Mohammed Nasser, Beth Kempton, John Brigande, Trevor J McGill, Andre Terzic, Paula Amato & Shoukhrat Mitalipov. (2020) Deleterious mtDNA mutations are common in mature oocytes. Biology of Reproduction 102:3, pages 607-619.
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Meysam Moghbeli. (2019) Genetics of recurrent pregnancy loss among Iranian population. Molecular Genetics & Genomic Medicine 7:9.
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K. Németh, O. Darvasi, I. Likó, N. Szücs, S. Czirják, L. Reiniger, B. Szabó, P. A. Kurucz, L. Krokker, P. Igaz, A. Patócs & H. Butz. (2019) Next-generation sequencing identifies novel mitochondrial variants in pituitary adenomas. Journal of Endocrinological Investigation 42:8, pages 931-940.
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Jesse Slone, Baoheng Gui & Taosheng Huang. (2018) The current landscape for the treatment of mitochondrial disorders. Journal of Genetics and Genomics 45:2, pages 71-77.
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Jun Ma, Heidi Purcell, Lori Showalter & Kjersti M. Aagaard. (2015) Mitochondrial DNA sequence variation is largely conserved at birth with rare de novo mutations in neonates. American Journal of Obstetrics and Gynecology 212:4, pages 530.e1-530.e8.
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