Development and characterization of a mouse with profound biotinidase deficiency: A biotin-responsive neurocutaneous disorder

Molecular Genetics and Metabolism - Tập 102 - Trang 161-169 - 2011
Kirit Pindolia1,2, Megan Jordan1, Caiying Guo3, Nell Matthews4, Donald M. Mock5,6, Erin Strovel7, Miriam Blitzer7, Barry Wolf1,2
1Department of Medical Genetics, Henry Ford Hospital, Detroit, MI 48202 USA
2Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI 48201, USA
3Howard Hughes Medical Institute, Janelia Farm, Ashburn, VA 20147, USA
4Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205. USA
5Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA
6Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR 72205 USA
7Division of Human Genetics, Department of Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA

Tài liệu tham khảo

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