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Q21198726-DABA17B8-96E7-4189-8354-C73AECBBBBC8
Q21198726-DABA17B8-96E7-4189-8354-C73AECBBBBC8
BestRank
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http://www.wikidata.org/entity/statement/Q21198726-DABA17B8-96E7-4189-8354-C73AECBBBBC8
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
P2860
Q21198726-DABA17B8-96E7-4189-8354-C73AECBBBBC8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21198726-DABA17B8-96E7-4189-8354-C73AECBBBBC8
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wasDerivedFrom
73bd439447ac64ac50f3d3fbc2e3923cb60c17e0
P2860
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease.