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Novel XK mutation in a McLeod patient diagnosed after heart transplant.

Clinical neurology and neurosurgery - 1 May 2018

Laurencin Chloé, Sebbag Laurent, Jousserand Guillemette, Demontes Marie, Campean Lia, Thivolet-Bejui Francoise, Lebre Anne Sophie, Thobois Stephane

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Identifiers

PMID: 29524658
DOI: 10.1016/j.clineuro.2018.02.039

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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"Acquired" sudden cardiac death high-risk genetic mutation in a heart transplant recipient.Semantic proximity Read ↗

A deCIDEdly New Germline Mutation That Protects Against Liver Disease.Semantic proximity Read ↗

BTKbase: XLA-mutation registry.Semantic proximity Read ↗

Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases.Semantic proximity Read ↗

Unmasking of novel mutations within <i>XK</i> gene that could be used as Diagnostic Markers to Predict McLeod syndrome: Using in silico analysisSemantic proximity Read ↗

BTKbase: a database of XLA-causing mutations. International Study Group.Semantic proximity Read ↗

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