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Heterozygous missense variants of LMX1A lead to nonsyndromi..:
DOOFNL Consortium
;
Wesdorp, Mieke
;
de Koning Gans, Pia A. M.
...
Human Genetics. 137 (2018) 5 - p. 389-400 , 2018
Link:
https://doi.org/10.1007/s00439-018-1880-5
RT Journal T1
Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00439-018-1880-5&Exemplar=1&LAN=DE A1 DOOFNL Consortium A1 Wesdorp, Mieke A1 de Koning Gans, Pia A. M. A1 Schraders, Margit A1 Oostrik, Jaap A1 Huynen, Martijn A. A1 Venselaar, Hanka A1 Beynon, Andy J. A1 van Gaalen, Judith A1 Piai, Vitória A1 Voermans, Nicol A1 van Rossum, Michelle M. A1 Hartel, Bas P. A1 Lelieveld, Stefan H. A1 Wiel, Laurens A1 Verbist, Berit A1 Rotteveel, Liselotte J. A1 van Dooren, Marieke F. A1 Lichtner, Peter A1 Kunst, Henricus P. M. A1 Feenstra, Ilse A1 Admiraal, Ronald J. C. A1 Yntema, Helger G. A1 Hoefsloot, Lies H. A1 Pennings, Ronald J. E. A1 Kremer, Hannie PB Springer Science and Business Media LLC YR 2018 SN 0340-6717 SN 1432-1203 JF Human Genetics VO 137 IS 5 SP 389 OP 400 LK http://dx.doi.org/https://doi.org/10.1007/s00439-018-1880-5 DO https://doi.org/10.1007/s00439-018-1880-5 SF ELIB - SuUB Bremen
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