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1 Ergebnisse
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Loss-of-function mutations in TDRD7 lead to a rare novel sy..:
Tan, Yue-Qiu
;
Tu, Chaofeng
;
Meng, Lanlan
...
Genetics in Medicine. 21 (2019) 5 - p. 1209-1217 , 2019
Link:
https://doi.org/10.1038/gim.2017.130
RT Journal T1
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_gim.2017.130&Exemplar=1&LAN=DE A1 Tan, Yue-Qiu A1 Tu, Chaofeng A1 Meng, Lanlan A1 Yuan, Shimin A1 Sjaarda, Calvin A1 Luo, Aixiang A1 Du, Juan A1 Li, Wen A1 Gong, Fei A1 Zhong, Changgao A1 Deng, Han-Xiang A1 Lu, Guangxiu A1 Liang, Ping A1 Lin, Ge PB Elsevier BV YR 2019 SN 1098-3600 JF Genetics in Medicine VO 21 IS 5 SP 1209 OP 1217 LK http://dx.doi.org/https://doi.org/10.1038/gim.2017.130 DO https://doi.org/10.1038/gim.2017.130 SF ELIB - SuUB Bremen
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