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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1996 3
1999 1
2000 1
2001 1
2002 1
2003 1
2004 1
2012 1
2020 1
2021 1
2024 0

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PubMed (cited) for id: 602538

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Page 1
De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy.
Itai T, Hamanaka K, Sasaki K, Wagner M, Kotzaeridou U, Brösse I, Ries M, Kobayashi Y, Tohyama J, Kato M, Ong WP, Chew HB, Rethanavelu K, Ranza E, Blanc X, Uchiyama Y, Tsuchida N, Fujita A, Azuma Y, Koshimizu E, Mizuguchi T, Takata A, Miyake N, Takahashi H, Miyagi E, Tsurusaki Y, Doi H, Taguri M, Antonarakis SE, Nakashima M, Saitsu H, Miyatake S, Matsumoto N. Itai T, et al. Hum Mutat. 2021 Jan;42(1):66-76. doi: 10.1002/humu.24130. Epub 2020 Nov 10. Hum Mutat. 2021. PMID: 33131106
Myotonic dystrophy: discussion of molecular mechanism.
Caskey CT, Swanson MS, Timchenko LT. Caskey CT, et al. Cold Spring Harb Symp Quant Biol. 1996;61:607-14. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246487 Review. No abstract available.
12 results