Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia (Q34205653)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia |
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Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia (English)
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Carsten Bergmann
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Klaus Zerres
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Sabine Rudnik-Schoneborn
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Thomas Eggermann
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Martin Häusler
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Michael Mull
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Vincent T Ramaekers
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21 May 2003
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126
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Pt 7
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1537-1544
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Identifiers
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