(Q55054635)

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A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. (English)

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

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Isabelle Schrauwen

2

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

8

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

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Effat Farrokhi

6

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Morteza Hashemzadeh Chaleshtori

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Morteza Hashemzadeh Chaleshtori

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Maarten Vanwesemael

1

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

Ruben Ceuppens

3

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

Fatemeh Alasti

4

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

Ellen Jorssen

5

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

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7 July 2011

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

American Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

155A

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

8

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

2021-2023

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Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34096

21 January 2018

A catechol-O-methyltransferase that is essential for auditory function in mice and humans

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34096

21 January 2018

Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34096

21 January 2018

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34096

21 January 2018

Identifiers

10.1002/AJMG.A.34096

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/21739586

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