Article Text
Online mutation report
Broader geographical spectrum of Cohen syndrome due to COH1 mutations
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Footnotes
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GHM is supported by the Charles H. Hood Foundation as a Medical Foundation Research Fellow, and by the William Randolph Hearst Fund. CAW is supported by grants from the National Institute of Neurological Disease and Stroke (2R37NS35129 and P01NS39404), the March of Dimes, and the McKnight Foundation.
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Conflict of interest: none declared.
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↵* These authors contributed equally to this work.