No abstract available
MeSH terms
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Amelogenesis Imperfecta / complications
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Amelogenesis Imperfecta / diagnosis*
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Amelogenesis Imperfecta / genetics
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Dementia / complications
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Dementia / diagnosis*
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Dementia / genetics
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Epilepsy / complications
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Epilepsy / diagnosis*
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Epilepsy / genetics
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Epilepsy, Generalized / genetics*
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Female
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Humans
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Mutation
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Symporters / genetics
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Tooth Abnormalities / genetics*
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Young Adult
Substances
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SLC13A5 protein, human
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Symporters
Supplementary concepts
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Kohlschutter Tonz syndrome