reference/21927796

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21927796

Outgoing Links

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endingPage	362
issn	1460-2083
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pageRange	355-362
publicationName	Human Molecular Genetics
startingPage	355
bibliographicCitation	Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Deutman AF, Hoyng CB. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR. Hum Mol Genet. 1998 Mar;7(3):355–62. doi: 10.1093/hmg/7.3.355. PMID: 9466990.
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date	1998-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/9466990 https://doi.org/10.1093/hmg/7.3.355
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR
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