No abstract available
MeSH terms
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Alleles
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Child, Preschool
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Choline-Phosphate Cytidylyltransferase / genetics*
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Choline-Phosphate Cytidylyltransferase / metabolism
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Female
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Humans
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Infant
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Male
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Middle Aged
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Mutation, Missense*
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Osteochondrodysplasias / genetics*
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Pedigree
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Phosphatidylcholines / metabolism*
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Retinitis Pigmentosa / genetics*
Substances
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Phosphatidylcholines
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Choline-Phosphate Cytidylyltransferase
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PCYT1A protein, human
Supplementary concepts
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Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy