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Fig. 5 | Journal of Neurodevelopmental Disorders

Fig. 5

From: Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder

Fig. 5

Quantification of whole blood GHB content in aldh5a1lox − STOP mice. GHB analyses of whole blood obtained from wild-type (WT), heterozygous (HET), and homozygous mutant (HOM) aldh5a1lox − STOP mice at postnatal age of 16 days. Quantification of GHB is expressed as µM. Individual data points, group mean, and SEM are shown. ****p < 0.0001, One-way ANOVA followed by Dunnett’s multiple comparisons test. Both male and female mice were used. n = 9 WT, 19 HET, 7 HOM mice

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