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Article

Coexisting PTPN11 and TNNT2 mutations in noonan syndrome with multiple lentigines.

QJM : monthly journal of the Association of Physicians - 25 Jun 2024

Liu H, Han X, Chu S, Ma W, Ding W, Li J, Jiang Y

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Share to Mutation
Share to N-Acetylglucosaminyltransferases
Share to Noonan Syndrome
Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 38366647
DOI: 10.1093/qjmed/hcae029

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

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Coexisting PTPN11 and TNNT2 mutations in noonan syndrome with multiple lentigines.PMID 38366647Read ↗

A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndromeSemantic proximity Read ↗

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Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 GeneSemantic proximity Read ↗

Hypertrophic neuropathy in Noonan syndrome with multiple lentigines.Semantic proximity Read ↗

Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants.Semantic proximity Read ↗

Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutationSemantic proximity Read ↗

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.Semantic proximity Read ↗

A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines.Semantic proximity Read ↗

Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines.Semantic proximity Read ↗

Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications.Semantic proximity Read ↗

Noonan syndrome and related disorders: genetics and pathogenesis.Semantic proximity Read ↗

Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome.Semantic proximity Read ↗

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