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Severe mutations in the ABCR gene are associated with a clinical subtype of autosomal recessive retinitis pigmentosa


Severe mutations in the ABCR gene are associated with a clinical subtype of autosomal recessive retinitis pigmentosa



American Journal of Human Genetics 65(4): A290



ISSN/ISBN: 0002-9297


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(PDF emailed within 1 workday: $29.90)

Accession: 035720887

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Related references

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