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Q30670235-84A00F8F-8BF0-4EA7-A660-293CB76EBA38
Q30670235-84A00F8F-8BF0-4EA7-A660-293CB76EBA38
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Statement
http://www.wikidata.org/entity/statement/Q30670235-84A00F8F-8BF0-4EA7-A660-293CB76EBA38
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
P2860
Q30670235-84A00F8F-8BF0-4EA7-A660-293CB76EBA38
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30670235-84A00F8F-8BF0-4EA7-A660-293CB76EBA38
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wasDerivedFrom
e35a45a012864338047f92b719e75805686e4bd2
P2860
Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report.