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Epidemiology of neurofibromatosis type 1 (NF1) in northern Finland

1 Aug 2000

Abstract excerpt

Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome EDITOR-Rett syndrome (RTT, MIM 312760) is a neurodevelopmental disorder characterised by normal early psychomotor development followed by a period of regression, the loss of acquired purposeful manual and speech skills, hand wringing, gait disturbance, and growth retardation. 1 As RTT occurs exclusively in females...

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PMID: 10991696
DOI: 10.1136/jmg.37.8.632

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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