Associated Papers
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.
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39962046 (PubMed )
Supplement: 41467_2025_56876_MOESM3_ESM.xlsx › Table_S1
Malakoplakia with aberrant ALK expression by immunohistochemistry: a case report.
Zhang XY et al.
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De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1312.477
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