DOI: 10.1086/378566. Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

10.1086/378566

Crossref journal-article

Elsevier BV

The American Journal of Human Genetics (78)

Bibliography

Bachinski, L. L., Udd, B., Meola, G., Sansone, V., Bassez, G., Eymard, B., Thornton, C. A., Moxley, R. T., Harper, P. S., Rogers, M. T., Jurkat-Rott, K., Lehmann-Horn, F., Wieser, T., Gamez, J., Navarro, C., Bottani, A., Kohler, A., Shriver, M. D., Sallinen, R., â¦ Krahe, R. (2003). Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect. The American Journal of Human Genetics, 73(4), 835â848.

Authors 23

Linda L. Bachinski (first)
Bjarne Udd (additional)
Giovanni Meola (additional)
Valeria Sansone (additional)
Guillaume Bassez (additional)
Bruno Eymard (additional)
Charles A. Thornton (additional)
Richard T. Moxley (additional)
Peter S. Harper (additional)
Mark T. Rogers (additional)
Karin Jurkat-Rott (additional)
Frank Lehmann-Horn (additional)
Thomas Wieser (additional)
Josep Gamez (additional)
Carmen Navarro (additional)
Armand Bottani (additional)
Andre Kohler (additional)
Mark D. Shriver (additional)
Riitta Sallinen (additional)
Maija Wessman (additional)
Shanxiang Zhang (additional)
Fred A. Wright (additional)
Ralf Krahe (additional)

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Dates

Type	When
Created	21 years, 10 months ago (Sept. 26, 2003, 12:28 p.m.)
Deposited	4 years, 2 months ago (June 11, 2021, 10:30 a.m.)
Indexed	3 weeks, 1 day ago (Aug. 2, 2025, 12:51 a.m.)
Issued	21 years, 10 months ago (Oct. 1, 2003)
Published	21 years, 10 months ago (Oct. 1, 2003)
Published Print	21 years, 10 months ago (Oct. 1, 2003)

Funders 0

None

BibTeX

@article{Bachinski_2003, title={Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect}, volume={73}, ISSN={0002-9297}, url={http://dx.doi.org/10.1086/378566}, DOI={10.1086/378566}, number={4}, journal={The American Journal of Human Genetics}, publisher={Elsevier BV}, author={Bachinski, Linda L. and Udd, Bjarne and Meola, Giovanni and Sansone, Valeria and Bassez, Guillaume and Eymard, Bruno and Thornton, Charles A. and Moxley, Richard T. and Harper, Peter S. and Rogers, Mark T. and Jurkat-Rott, Karin and Lehmann-Horn, Frank and Wieser, Thomas and Gamez, Josep and Navarro, Carmen and Bottani, Armand and Kohler, Andre and Shriver, Mark D. and Sallinen, Riitta and Wessman, Maija and Zhang, Shanxiang and Wright, Fred A. and Krahe, Ralf}, year={2003}, month=oct, pages={835–848} }

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