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Article

Electrocardiography in Noonan syndrome PTPN11 gene mutation--phenotype characterization.

American journal of medical genetics. Part A - 1 Feb 2008

Croonen Ellen A, van der Burgt Ineke, Kapusta Livia, Draaisma Jos M Th

Abstract excerpt

Noonan syndrome is a developmental disorder with distinctive facial features, short stature and cardiac abnormalities. In this cross-sectional study, we evaluated characteristic electrocardiographic (ECG) findings and cardiac abnormalities in 84 patients with Noonan syndrome, 56 (67%) of who were...

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Source

Identifiers

PMID: 18203203
DOI: 10.1002/ajmg.a.32140

Genes

PTPN11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18203203-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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