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A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family

scientific article published on 03 October 2012

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A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family (English)

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10 March 2020

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Seema Saini

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1

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Jai Rup Singh

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Vanita Vanita

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3 October 2012

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Experimental Eye Research

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23041261

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104

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82-88

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10.1016/J.EXER.2012.09.010

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23041261

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23041261%20AND%20SRC:MED&resulttype=core&format=json

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10 March 2020

PubMed publication ID

23041261

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23041261

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23041261%20AND%20SRC:MED&resulttype=core&format=json

(Q56988670)

A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family

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