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It might help you to print off the documents in the links I left, read through, and highlight anything that is relevant to your case, paying particular attention to: problems with serum B12 testing - especially once treatment has commenced, BSH guidelines for treatment - especially where neurological symptoms are concerned, the role (or not) of macrocytic anaemia, and the important of treating symptoms (not serum B12 levels or on the presence/absence of macrocytic anaemia)

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A recent genome-wide study of monoallelically expressed genes from ASD samples, however, revealed heterogeneity that confounds the link between parental imprinting and ASD risk [106]

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