(Q80750907)

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A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity

scientific article published on 26 July 2007

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17679936

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A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity (English)

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Europe PubMed Central

PubMed ID

17679936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17679936%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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Luz M Gonzalez-Huerta

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1

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17679936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17679936%20AND%20SRC:MED&resulttype=core&format=json

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3 January 2020

Olga M Messina-Baas

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2

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17679936

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3 January 2020

Sergio A Cuevas-Covarrubias

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3

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17679936

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3 January 2020

publication date

26 July 2007

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17679936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17679936%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

Europe PubMed Central

PubMed ID

17679936

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17679936%20AND%20SRC:MED&resulttype=core&format=json

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3 January 2020

volume

13

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17679936

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3 January 2020

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1333-1338

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17679936

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3 January 2020

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PubMed ID

17679936

1 reference

stated in

Europe PubMed Central

PubMed ID

17679936

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17679936%20AND%20SRC:MED&resulttype=core&format=json

(Q80750907)

A family with autosomal dominant primary congenital cataract associated with a CRYGC mutation: evidence of clinical heterogeneity

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