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Article

Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome.

Pediatric neurology - 1 Mar 2002

Khong Pek Lan, Lam Ching Wan, Ooi Clara G C, Ko Chun Hung, Wong Virginia C N

Abstract excerpt

We studied the in vivo cerebral metabolites and documented the presence of MECP2 gene mutations in six Chinese females with Rett syndrome. Magnetic resonance spectroscopy spectra from the frontal lobe (gray and white matter) and deep gray nuclei (basal ganglia and thalamus) of either side were obtained. N-acetylaspartate/total creatine, choline/total creatine, and N-acetylaspartate/choline ratios were analyzed...

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Source

Identifiers

PMID: 11955928
DOI: 10.1016/s0887-8994(01)00385-x

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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