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Family study on mitochondrial DNA polymorphism

Harihara, S.; Nakamura, T.; Harada, S.; Asaka, A.; Omoto, K.; Misawa, S.

Nihon Hoigaku Zasshi 43(3): 257-261

1989

ISSN/ISBN: 0047-1887
PMID: 2572712
Document Number: 343922
Mitochondrial DNA restriction fragment length polymorphisms (mtDNA RFLPs) were surveyed among 19 Japanese families with 67 individuals including twins. A mother and children, and siblings of each family showed the same pattern of mtDNA RFLPs. Samples from Japanese war orphans remained in China and their probable relatives were also surveyed and one pair indicating a high probability to be siblings using other genetic markers possessed the same variant of mtDNA. Moreover mtDNA RFLPs was applied for maternity test among two families. The data suggested that parents mistook their children for each other at birth.

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Bermisheva, M.A.; Viktorova, T.V.; Khusnutdinova, E.K. 2003: Polymorphism of human mitochondrial DNA Genetika 39(8): 1013-1025
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De Benedictis, G.; Rose, G.; Cacciò, S.; Picardi, P.; Quagliariello, C. 1989: Mitochondrial DNA polymorphism in Calabria (southern Italy) Gene Geography: a Computerized Bulletin on Human Gene Frequencies 3(1): 33-40
Naumova, E.S.; Naumov, G.I.; Barrio, E.; Querol, A. 2010: Mitochondrial DNA polymorphism of the yeast Saccharomyces bayanus var. uvarum Mikrobiologiia 79(4): 543-550
Paweł, K.; Hauser, J.; Skibińska, M.; Szczepankiewicz, A.; Dmitrzak-Weglarz, M.; Gorzkowska, K.; Pawlak, J.; Czerski, P.M. 2010: Family based association study of DRD1, DRD2, DRD3, DRD4, DAT, COMT gene polymorphism in schizophrenia Psychiatria Polska 44(3): 405-413
Maliarchuk, B.A.; Derenko, M.V. 1995: Polymorphism of mitochondrial DNA region V in native and migrant inhabitants of Northeast Asia Genetika 31(9): 1308-1313
Song, D.; Zhang, Y.; Shi, J. 2001: The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies Zhonghua Yi Xue Za Zhi 81(11): 659-661
Maliarchuk, B.A.; Perkova, M.A.; Derenko, M.V. 2011: Polymorphism of 5' promotor region of mitochondrial gamma-DNA-polymerase gene in human populations Molekuliarnaia Biologiia 45(5): 924-926
Yacoubi Loueslati, B.; Ennafaa, H.; Ben Amor, M.; Heyer, E.; Langaney, A.; Ben Ayed, F.; Ben Ammar Elgaaied, A. 1998: Mitochondrial DNA polymorphism reveals a genetic differentiation between ethnic groups in the population of Jerba Archives de l'Institut Pasteur de Tunis 75(1-2): 9-18
Kornienko, I.V.; Vodolazhskiĭ, D.I.; Kornienko, I.E.; Ivanov, P.L. 2004: Polymorphism of structural genes of human mitochondrial DNA for forensic medical personal identification Sudebno-Meditsinskaia Ekspertiza 47(3): 11-15
Bermisheva, M.A.; Viktorova, T.V.; Beliaeva, O.; Limborskaia, S.A.; Khusnutdinova, E.K. 2001: Polymorphism of hypervariable segment i of mitochondrial DNA in three ethnic groups of the Volga-Ural region Genetika 37(8): 1118-1124
Robitaille, J.; Després, J-P.; Pérusse, L.; Vohl, M-C. 2003: The PPAR-gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: results from the Québec Family Study Clinical Genetics 63(2): 109-116
Nikulina, S.I.; Shul'man, V.A.; Vorotnikova, I.V.; Puzyrev, V.P.; Kosiankova, T.V.; Golubenko, M.V. 2003: Relationship between polymorphism of non-coding regions of human mitochondrial genome and primary cardiac conduction disorders Terapevticheskii Arkhiv 75(10): 75-77
Ohta, S. 1995: Mitochondrial diseases caused by mitochondrial DNA mutants and their related regulation of mitochondrial biogenesis Seikagaku. Journal of Japanese Biochemical Society 67(1): 15-32
Marsac, C.; Degoul, F.; Bonne, G.; Romero, N.; Nelson, I.; Fardeau, M.; François, D.; Ponsot, G.; Harpey, J.P.; Eymard, B. 1991: Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy Revue Neurologique (Paris) 147(6-7): 462-466
Inamori, M.; Ishigami, T.; Takahashi, N.; Hibi, K.; Ashino, K.; Sumita, S.; Tamura, K.; Ochiai, H.; Umemura, S.; Ishii, M.; Tanaka, S.; Sekihara, H.; Inayama, Y. 1997: A case of mitochondrial cardiomyopathy with heart failure, sick sinus syndrome and diabetes mellitus: mitochondrial DNA adenine-to-guanine transition at 3243 of mitochondrial tRNA(LEU)(UUR) gene Journal of Cardiology 30(6): 341-347
Petrishchev, V.N.; Kutueva, A.B.; Rychkov, I.G. 1993: Deletion-insertion polymorphism in the V-region of mitochondrial DNA in ten Mongoloid populations of Siberia, Frequency of deletion correlates with the geographic coordinates of the locality Genetika 29(7): 1196-1204
Elverland, H.H.; Torbergsen, T. 1991: Audiologic findings in a family with mitochondrial disorder American Journal of Otology 12(6): 459-465
Fajardo, V.; González, I.; López-Calleja, Iés.; Martin, I.; Rojas, M.; Pavón, M.Angel.; Hernández, P.E.; García, T.; Martín, R. 2007: Analysis of mitochondrial DNA for authentication of meats from chamois (Rupicapra rupicapra), pyrenean ibex (Capra pyrenaica), and mouflon (Ovis ammon) by polymerase chain reaction-restriction fragment length polymorphism Journal - Association of Official Analytical Chemists 90(1): 179-186
Kawai, H.; Akaike, M.; Yokoi, K.; Tamaki, Y.; Saito, S. 1993: Mitochondrial myopathy with autosomal dominant inheritance--report of a family and review of the literature Rinsho Shinkeigaku 33(2): 162-168