Wikidata

(Q43218224)

English

A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration

scientific article published in January 1999

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Statements

title
A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration (English)
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
author name string
A K Lalwani
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
W M Luxford
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
A N Mhatre
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
A Attaie
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
E R Wilcox
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
C M Castelein
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
publication date
1 January 1999
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
volume
64
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017
page(s)
318-323
1 reference
stated in
Europe PubMed Central
PMCID
1377736
retrieved
16 November 2017

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