Publication | Open Access
High frequency of<i>HTRA1</i>AND<i>ABCC6</i>mutations in Japanese patients with adult-onset cerebral small vessel disease
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Citations
29
References
2022
Year
More than 90% of mgCSVDs were diagnosed by screening for <i>NOTCH3</i>, <i>HTRA1</i> and <i>ABCC6</i>. The target sequences for these three genes may efficiently diagnose mgCSVD in Japanese patients.
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