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

M Wesdorp; P Gans; M Schraders; J Oostrik; MA Huynen; H Venselaar; AJ Beynon; J van Gaalen; V Piai; N Voermans; MM van Rossum; B P Hartel; SH Lelieveld; L Wiel; B Verbist; LJ Rotteveel; Marieke van Dooren; P Lichtner; HPM Kunst; I Feenstra; RJC Admiraal; HG Yntema; EH Hoefsloot; RJE Pennings; H Kremer

doi:10.1007/s00439-018-1880-5

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

M Wesdorp, P Gans, M Schraders, J Oostrik, MA Huynen, H Venselaar, AJ Beynon, J van Gaalen, V Piai, N Voermans, MM van Rossum, B P Hartel, SH Lelieveld, L Wiel, B Verbist, LJ Rotteveel, Marieke van Dooren, P Lichtner, HPM Kunst, I FeenstraRJC Admiraal, HG Yntema, EH Hoefsloot, RJE Pennings, H Kremer

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

21 Citations (Scopus)

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Original language	Undefined/Unknown
Pages (from-to)	389-400
Number of pages	12
Journal	Human Genetics
Volume	137
Issue number	5
DOIs	https://doi.org/10.1007/s00439-018-1880-5
Publication status	Published - 2018

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http://hdl.handle.net/1765/106391

Cite this

Wesdorp, M., Gans, P., Schraders, M., Oostrik, J., Huynen, MA., Venselaar, H., Beynon, AJ., van Gaalen, J., Piai, V., Voermans, N., van Rossum, MM., Hartel, B. P., Lelieveld, SH., Wiel, L., Verbist, B., Rotteveel, LJ., van Dooren, M., Lichtner, P., Kunst, HPM., ... Kremer, H. (2018). Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction. Human Genetics, 137(5), 389-400. https://doi.org/10.1007/s00439-018-1880-5

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title = "Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction",

author = "M Wesdorp and P Gans and M Schraders and J Oostrik and MA Huynen and H Venselaar and AJ Beynon and {van Gaalen}, J and V Piai and N Voermans and {van Rossum}, MM and Hartel, {B P} and SH Lelieveld and L Wiel and B Verbist and LJ Rotteveel and {van Dooren}, Marieke and P Lichtner and HPM Kunst and I Feenstra and RJC Admiraal and HG Yntema and EH Hoefsloot and RJE Pennings and H Kremer",

year = "2018",

doi = "10.1007/s00439-018-1880-5",

language = "Undefined/Unknown",

volume = "137",

pages = "389--400",

journal = "Human Genetics",

issn = "0340-6717",

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Wesdorp, M, Gans, P, Schraders, M, Oostrik, J, Huynen, MA, Venselaar, H, Beynon, AJ, van Gaalen, J, Piai, V, Voermans, N, van Rossum, MM, Hartel, BP, Lelieveld, SH, Wiel, L, Verbist, B, Rotteveel, LJ, van Dooren, M, Lichtner, P, Kunst, HPM, Feenstra, I, Admiraal, RJC, Yntema, HG, Hoefsloot, EH, Pennings, RJE & Kremer, H 2018, 'Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction', Human Genetics, vol. 137, no. 5, pp. 389-400. https://doi.org/10.1007/s00439-018-1880-5

TY - JOUR

T1 - Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

AU - Wesdorp, M

AU - Gans, P

AU - Schraders, M

AU - Oostrik, J

AU - Huynen, MA

AU - Venselaar, H

AU - Beynon, AJ

AU - van Gaalen, J

AU - Piai, V

AU - Voermans, N

AU - van Rossum, MM

AU - Hartel, B P

AU - Lelieveld, SH

AU - Wiel, L

AU - Verbist, B

AU - Rotteveel, LJ

AU - van Dooren, Marieke

AU - Lichtner, P

AU - Kunst, HPM

AU - Feenstra, I

AU - Admiraal, RJC

AU - Yntema, HG

AU - Hoefsloot, EH

AU - Pennings, RJE

AU - Kremer, H

PY - 2018

Y1 - 2018

U2 - 10.1007/s00439-018-1880-5

DO - 10.1007/s00439-018-1880-5

M3 - Article

SN - 0340-6717

VL - 137

SP - 389

EP - 400

JO - Human Genetics

JF - Human Genetics

IS - 5

ER -