(Q78526734)

English

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome

scientific article published on 14 September 2002

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Europe PubMed Central

PubMed ID

12436246

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

title

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

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Kathy King

1

1 reference

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

Frances A Flinter

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2

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

Vandana Nihalani

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3

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

Peter M Green

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4

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

publication date

14 September 2002

1 reference

stated in

Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference

Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

volume

111

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

issue

6

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Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

page(s)

548-554

1 reference

stated in

Europe PubMed Central

PubMed ID

12436246

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12436246%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 December 2019

exact match

https://scigraph.springernature.com/pub.10.1007/s00439-002-0830-3

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(Q78526734)

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome

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