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Homo sapiens chromosome 4, GRCh38.p14 Primary Assembly

NCBI Reference Sequence: NC_000004.12

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  • Homo sapiens chromosome 4, GRCh38.p14 Primary Assembly
    Homo sapiens chromosome 4, GRCh38.p14 Primary Assembly
    gi|568815594|gnl|ASM:GCF_000001305| |NC_000004.12||gpp|GPC_000001296.1||gnl|NCBI_GENOMES|4
    Nucleotide
  • Retinitis Pigmentosa
    Retinitis Pigmentosa
    Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition ...<br/>
    MeSH

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