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Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

Mieke Wesdorp; Pia A. M. de Koning Gans; Margit Schraders; Jaap Oostrik; Martijn A. Huynen; Hanka Venselaar; Andy J. Beynon; Judith van Gaalen; Vitória Piai; Nicol Voermans; Michelle M. van Rossum; Bas P. Hartel; Stefan H. Lelieveld; Laurens Wiel; Berit Verbist; Liselotte J. Rotteveel; Marieke F. van Dooren; Peter Lichtner; Henricus P. M. Kunst; Ilse Feenstra; Ronald J. C. Admiraal; Helger G. Yntema; Lies H. Hoefsloot; Ronald J. E. Pennings; Hannie Kremer
Human Genetics · Vol. 137, Issue 5 · pp. 389-400 · 2018

Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2018-05-01
Publication Year2018
Volume137
Issue5
Pages389-400
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-018-1880-5

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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