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Article

An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta.

Journal of medical genetics - 1 Jun 2004

Michaelides M, Bloch-Zupan A, Holder G E, Hunt D M, Moore A T

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Share to Amelogenesis Imperfecta
Share to Chromosomes, Human, Pair 2
Share to Corneal Dystrophies, Hereditary
Share to Cyclic Nucleotide-Gated Cation Channels

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Photoreceptor Cells, Vertebrate

Share to Retinal Degeneration

Source

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Identifiers

PMID: 15173235
DOI: 10.1136/jmg.2003.015792
PMCID: PMC1735797

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