(Q28218593)

English

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)

scientific article (publication date: June 2002)

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title

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture) (English)

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author name string

Richard G Weleber

series ordinal

1

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language of work or name

English

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publication date

June 2002

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published in

Ophthalmic Genetics

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volume

23

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issue

2

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page(s)

71-97

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cites work

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene

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https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

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21 January 2018

Leber’s Congenital Amaurosis as Conceived by Leber

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https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis

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reference URL

https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis

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Crossref

reference URL

https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

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https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

Ueber Retinitis pigmentosa und angeborene Amaurose

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https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses

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reference URL

https://api.crossref.org/works/10.1076%2FOPGE.23.2.71.2214

retrieved

21 January 2018

Identifiers

DOI

10.1076/OPGE.23.2.71.2214

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PubMed ID

12187427

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(Q28218593)

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)

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