Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families. (Q51933512)
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scientific article published in January 2005
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families. |
scientific article published in January 2005 |
Statements
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families. (English)
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Mancini GM
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Catsman-Berrevoets CE
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de Coo IF
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Aarsen FK
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Kamphoven JH
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Huijmans JG
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Duran M
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van der Knaap MS
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Jakobs C
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Salomons GS
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1 January 2005
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132A
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288-295
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