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Citations to this article

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.
N Narita, … , H Nakamura, M Matsuo
N Narita, … , H Nakamura, M Matsuo
Published May 1, 1993
Citation Information: J Clin Invest. 1993;91(5):1862-1867. https://doi.org/10.1172/JCI116402.
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Research Article

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.

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Abstract

Authors

N Narita, H Nishio, Y Kitoh, Y Ishikawa, Y Ishikawa, R Minami, H Nakamura, M Matsuo

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Total citations by year

Year: 2025 2023 2022 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 2001 2000 1999 1998 1997 1996 1995 1994 1993 1991 Total
Citations: 1 3 2 2 2 3 5 7 3 6 10 5 6 6 1 1 4 6 5 3 4 5 3 7 7 13 9 11 10 8 2 1 161
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article in year 2011 (6)

Title and authors Publication Year
Genome-wide analysis of mobile genetic element insertion sites
K Rawal, R Ramaswamy
Nucleic Acids Research 2011
On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease
DN Cooper, A Bacolla, C Férec, KM Vasquez, H Kehrer-Sawatzki, JM Chen
Human Mutation 2011
L1 Hybridization Enrichment: A Method for Directly Accessing De Novo L1 Insertions in the Human Germline
P Freeman, C Macfarlane, P Collier, AJ Jeffreys, RM Badge
Human Mutation 2011
Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4
B Baskin, WT Gibson, PN Ray
Neuromuscular Disorders 2011
Pathogenic orphan transduction created by a non-reference LINE-1 retrotransposon
S Solyom, AD Ewing, DC Hancks, Y Takeshima, H Awano, M Matsuo, HH Kazazian
Human Mutation 2011
LINE-1 elements in structural variation and disease
CR Beck, JL Garcia-Perez, RM Badge, JV Moran
Annual Review of Genomics and Human Genetics 2011

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