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- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion type Assertion NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_head.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion description "[The authors report detailed clinical and developmental assessment of 3 brothers who were found to carry a novel mutation in the ARX gene associated with a relatively mild phenotype of static global developmental delay and early hand preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
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- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion SIO_000772 22922607 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
- NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_assertion wasDerivedFrom befree-20150227 NP978170.RAplBS1ob-DnHnsTCGTErzqDrSEV-JklrCdHnrNb-o48k130_provenance.
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