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De novo Mutations in NALCN Cause a Syndrome of Congenital... | ResearchHub
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De novo Mutations in NALCN Cause a Syndrome of Congenital Contractures of the Limbs and Face with Hypotonia, and Developmental Delay
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Authors
Jessica Chong
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Jessica Chong
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Jessica Chong
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Michael Bamshad
Published
January 11, 2015
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Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Missense Mutation
Hypotonia
Show all topics
DOI
10.1101/013656
License
CC-BY-NC
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Missense Mutation
Hypotonia
Show all topics
DOI
10.1101/013656
License
CC-BY-NC
Other Formats
PDF
