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Category SearchDevgan Syndrome: Pulmonary Fibrosis, Ataxia, Ocular Telangiectasia, Microcephaly, Immunodeficiency, and Growth Retardation Associated with Mutations in the DNA Repair Gene RNF168
Text Registration
Copyright Title
Devgan Syndrome: Pulmonary Fibrosis, Ataxia, Ocular Telangiectasia, Microcephaly, Immunodeficiency, and Growth Retardation Associated with Mutations in the DNA Repair Gene RNF168
Status
Published
on 26 Feb 2009
Year of Creation
2008
Copyright Claimant
Sue S. Devgan
Registration Number
TX0007037105
on 26 Feb 2009Copyright Summary
The U.S. Copyright record (Registration Number: TX0007037105) dated 26 Feb 2009, pertains to an electronic file (eService) titled "Devgan Syndrome: Pulmonary Fibrosis, Ataxia, Ocular Telangiectasia, Microcephaly, Immunodeficiency, and Growth Retardation Associated with Mutations in the DNA Repair Gene RNF168" created in 2008. The copyright holder is Sue S. Devgan, known for their creative contributions in text registration. For any inquiries concerning this copyrighted material, kindly reach out to Sue S. Devgan.
Application Details
Registration Number
TX0007037105
Registration Date
2/26/2009
Year of Creation
2008
Agency Marc Code
DLC-CO
Record Status
New
Physical Description
Electronic file
First Publication Nation
United States
Notes
Rights Note: Sue S. Devgan, 11735 W. Washington Blvd., Los Angeles, CA, 90066, United States
Local Copyright Note: Regarding author information: Research itself not copyrightable. Compendium II 318.01. Registration extends to new text deposited
Statements
Application Title Statement: Devgan Syndrome: Pulmonary Fibrosis, Ataxia, Ocular Telangiectasia, Microcephaly, Immunodeficiency, and Growth Retardation Associated with Mutations in the DNA Repair Gene RNF168
Author Statement: Sue S. Devgan Citizenship: United States Authorship: text, scientific and medical research
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