Neu-Laxova Syndrome Due to Phosphoserine Aminotransferase Deficiency

Alias:

Phosphoserine Aminotransferase Deficiency, Prenatal Form

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Gene & Mutation

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Neu-Laxova Syndrome Due to Phosphoserine Aminotransferase Deficiency, is also known as phosphoserine aminotransferase deficiency, prenatal form. An important gene associated with Neu-Laxova Syndrome Due to Phosphoserine Aminotransferase Deficiency is PSAT1 (Phosphoserine Aminotransferase 1). Affiliated tissues include skin and eye.

Related ID：

MALACARDS：NLX005