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Product

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

Center:

WA-Univ. of Washington PPC

Fiscal Year:

2012

Contact Information:

Product Description:

CONCLUSIONS: Mutations in DNAH11 are a common cause of PCD in patients without ciliary ultrastructural defects; thus, genetic analysis can be used to ascertain the diagnosis of PCD in this challenging group of patients.

Keyword(s):

PCD, Mutations of DNAH11

Product/Publication Type(s):

Peer-reviewed publications in scholarly journals Published/In Press

Target Audience:

Professionals

Alternative Format:

To Obtain Copies (URL or Email):

[email protected]

COVID-19 Related Data:

N/A

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