Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

Published 2019 View Full Article

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Title
Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms
Authors
Keywords
-
Journal
JOURNAL OF MEDICAL GENETICS
Volume -, Issue -, Pages jmedgenet-2018-105918
Publisher
BMJ
Online
2019-08-01
DOI
10.1136/jmedgenet-2018-105918

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