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Items: 3

1.
Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
P Szepetowski, J Rochette, P Berquin, C Piussan, G M Lathrop, A P Monaco
Am J Hum Genet. 1997 Oct; 61(4): 889–898. doi: 10.1086/514877
PMCID:
PMC1715981
SummaryPage BrowsePDF–1.5M
2.
Paroxysmal Kinesigenic Choreoathetosis Locus Maps to Chromosome 16p11.2-q12.1
Hiro-aki Tomita, Shinichiro Nagamitsu, Keiko Wakui, Yoshimitsu Fukushima, Koki Yamada, Miyuki Sadamatsu, Akira Masui, Tohru Konishi, Toyojiro Matsuishi, Masao Aihara, Katsunori Shimizu, Kiyoshi Hashimoto, Mari Mineta, Michihito Matsushima, Takahiro Tsujita, Masaaki Saito, Hajime Tanaka, Shoji Tsuji, Toshihisa Takagi, Yusuke Nakamura, Shinichiro Nanko, Nobumasa Kato, Yoshibumi Nakane, Norio Niikawa
Am J Hum Genet. 1999 Dec; 65(6): 1688–1697. Published online 1999 Nov 18. doi: 10.1086/302682
PMCID:
PMC1288380
AbstractArticlePDF–405K
3.
Base-resolution mapping reveals distinct m1A methylome in nuclear- and mitochondrial-encoded transcripts
Xiaoyu Li, Xushen Xiong, Meiling Zhang, Kun Wang, Ying Chen, Jun Zhou, Yuanhui Mao, Jia Lv, Danyang Yi, Xiao-Wei Chen, Chu Wang, Shu-Bing Qian, Chengqi Yi
Mol Cell. Author manuscript; available in PMC 2018 Dec 7.
Published in final edited form as: Mol Cell. 2017 Dec 7; 68(5): 993–1005.e9. Published online 2017 Nov 5. doi: 10.1016/j.molcel.2017.10.019
PMCID:
PMC5722686
AbstractArticlePDF–1.4M

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