(Q50475859)

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GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.

scientific article published in December 2004

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Europe PubMed Central

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15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

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6 January 2020

title

GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation (English)

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Europe PubMed Central

PubMed publication ID

15603707

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

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Zi-an Xiao

1

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Europe PubMed Central

PubMed publication ID

15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

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6 January 2020

Ding-hua Xie

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2

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Europe PubMed Central

PubMed publication ID

15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

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6 January 2020

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English

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1 December 2004

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15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 January 2020

published in

Chinese Medical Journal

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PubMed publication ID

15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

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6 January 2020

volume

117

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Europe PubMed Central

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15603707

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6 January 2020

issue

12

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Europe PubMed Central

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15603707

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

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6 January 2020

page(s)

1797-1801

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15603707

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retrieved

6 January 2020

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PubMed publication ID

15603707

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15603707

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15603707%20AND%20SRC:MED&resulttype=core&format=json

(Q50475859)

GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.

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