Wikidata

(Q43914098)

English

Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation

scientific article published in February 2002

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Statements

title
Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
author name string
Yuya Tamagawa
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Kazuhiro Ishikawa
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Kotaro Ishikawa
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Takashi Ishida
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Ken Kitamura
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Shinji Makino
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Tadahiko Tsuru
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
Keiichi Ichimura
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
publication date
1 February 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017
page(s)
292-297
1 reference
stated in
Europe PubMed Central
PubMed ID
11889386
retrieved
28 November 2017

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