Associated Papers
Novel KIF26A variants associated with pediatric intestinal pseudo-obstruction (PIPO) and brain developmental defects.
Nosrati MSS et al.
Clinical Genetics, 2025
Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families.
AlAbdi L et al.
Nature Communications, 2023
37644014 (PubMed )
Supplement: 41467_2023_40909_MOESM24_ESM.xlsx › Sheet1
KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon.
Almannai M et al.
Human Genetics, 2023
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