Phosphoserine aminotransferase deficiency (Q85502)
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Phosphoserine aminotransferase deficiency is an extremely rare form of serine deficiency syndrome characterised clinically in the two reported cases to date by acquired microcephaly, psychomotor retardation, intractable seizures and hypertonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1210469497 |
||
| English | Phosphoserine aminotransferase deficiency |
Phosphoserine aminotransferase deficiency is an extremely rare form of serine deficiency syndrome characterised clinically in the two reported cases to date by acquired microcephaly, psychomotor retardation, intractable seizures and hypertonia. |
