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Exome Sequencing Reveals De Novo WDR45 Mutations Causing ... | ResearchHub
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Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA
0
Authors
Tobias Haack
32 more
Tobias Haack
•
Penelope Hogarth
30 more
•
Susan Hayflick
Published
November 21, 2012
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Journal
The American Journal of Human Genetics
Topics
Biology
Hematology
Neurology
Molecular Biology
Phenotype
Show all topics
DOI
10.1016/j.ajhg.2012.10.019
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publisher-specific-oa
Supporters
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Journal
The American Journal of Human Genetics
Topics
Biology
Hematology
Neurology
Molecular Biology
Phenotype
Show all topics
DOI
10.1016/j.ajhg.2012.10.019
License
publisher-specific-oa
