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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2011 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 10973
3 results
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Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3.
HGG Adv. 2021 Jan 21;2(2):100024. doi: 10.1016/j.xhgg.2021.100024. eCollection 2021 Apr 8.
HGG Adv. 2021.
PMID: 35047834
Free PMC article.
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Najmabadi H, Hu H, Garshasbi M, Zemojtel T, Abedini SS, Chen W, Hosseini M, Behjati F, Haas S, Jamali P, Zecha A, Mohseni M, Püttmann L, Vahid LN, Jensen C, Moheb LA, Bienek M, Larti F, Mueller I, Weissmann R, Darvish H, Wrogemann K, Hadavi V, Lipkowitz B, Esmaeeli-Nieh S, Wieczorek D, Kariminejad R, Firouzabadi SG, Cohen M, Fattahi Z, Rost I, Mojahedi F, Hertzberg C, Dehghan A, Rajab A, Banavandi MJ, Hoffer J, Falah M, Musante L, Kalscheuer V, Ullmann R, Kuss AW, Tzschach A, Kahrizi K, Ropers HH.
Najmabadi H, et al.
Nature. 2011 Sep 21;478(7367):57-63. doi: 10.1038/nature10423.
Nature. 2011.
PMID: 21937992
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Novel transcription coactivator complex containing activating signal cointegrator 1.
Jung DJ, Sung HS, Goo YW, Lee HM, Park OK, Jung SY, Lim J, Kim HJ, Lee SK, Kim TS, Lee JW, Lee YC.
Jung DJ, et al.
Mol Cell Biol. 2002 Jul;22(14):5203-11. doi: 10.1128/MCB.22.14.5203-5211.2002.
Mol Cell Biol. 2002.
PMID: 12077347
Free PMC article.
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