(Q55043732)

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Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.

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29 December 2019

Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17431902%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

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Hossein Najmabadi

12

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29 December 2019

5

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29 December 2019

10

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29 December 2019

Richard J Smith

11

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29 December 2019

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Nicole C Meyer

1

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29 December 2019

Fatemeh Alasti

2

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29 December 2019

Carla J Nishimura

3

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Europe PubMed Central

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29 December 2019

Parisa Imanirad

4

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29 December 2019

Yasser Riazalhosseini

6

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29 December 2019

Mahdi Malekpour

7

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29 December 2019

Nafiseh Kochakian

8

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Europe PubMed Central

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29 December 2019

Payman Jamali

9

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29 December 2019

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1 July 2007

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29 December 2019

American Journal of Medical Genetics

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29 December 2019

143A

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29 December 2019

14

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29 December 2019

1623-1629

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29 December 2019

Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.31718

21 January 2018

Identifiers

10.1002/AJMG.A.31718

1 reference

Europe PubMed Central

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29 December 2019

PubMed publication ID

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Europe PubMed Central

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29 December 2019

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