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FilenameFormatSizeDescription
cge12018-sup-0001-TableS1.docWord document225KTable S1. Genes with rare missense, nonsense, or splice variants reported in NSCL/P.
cge12018-sup-0002-TableS2.docWord document183KTable S2. Variant positions for genes with updated RefSeq transcripts.
cge12018-sup-0003-TableS3.docWord document223KTable S3. Variants previously reported in NSCL/P cases and population or CEPH controls.

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