Complication begets clarification in classification
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/136/2/368/11139587/awt001.pdf
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3. An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation;Cederquist;Hum Mol Genet,2012
4. A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3;Chew;Brain,2013
5. Overlapping cortical malformations and mutations in TUBB2B and TUBA1A;Cushion;Brain,2013
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