Whole-exome sequencing associates novel <i>CSMD1</i> gene mutations with familial Parkinson disease.

Neurol Genet · 2017 · PMC5540655 · PMID 28808687

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highly significantno p-value reported

28 This association remained highly significant when including all PD (familial and sporadic) and sporadic PD cases.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.

Whole-exome sequencing associates novel &lt;i&gt;CSMD1&lt;/i&gt; gene mutations with familial Parkinson disease.

The sentences

Whole-exome sequencing associates novel <i>CSMD1</i> gene mutations with familial Parkinson disease.