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pro vyhledávání: '"Michael Snyder"'
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 12, Iss 5 (2022)
Abstract Caenorhabditis elegansC. elegansC. elegansUMrt ×−5 s¯
Externí odkaz:
https://doaj.org/article/d4f166ed846a44fdac9d8c64c54f7402
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Autor:
Lorelei D. Shoemaker, Michael J. Clark, Anil Patwardhan, Gemma Chandratillake, Sarah Garcia, Rong Chen, Alexander A. Morgan, Nan Leng, Scott Kirk, Richard Chen, Douglas J. Cook, Michael Snyder, Gary K. Steinberg
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 1, Pp 41-49 (2016)
Moyamoya disease (MMD) is a rare disorder characterized by cerebrovascular occlusion and development of hemorrhage-prone collateral vessels. Approximately 10–12% of cases are familial, with a presumed low penetrance autosomal dominant pattern of in
Externí odkaz:
https://doaj.org/article/b8e4c8ec6df84ba1a2dc5c4670dd6173
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Autor:
Gary K. Steinberg, Richard Chen, Michael Snyder, Douglas J. Cook, Michael J. Clark, Sarah Garcia, Nan Leng, Gemma Chandratillake, Alexander A. Morgan, Scott Kirk, Anil Patwardhan, Lorelei D. Shoemaker, Rong Chen
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 1, Pp 41-49 (2016)
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics
Moyamoya disease (MMD) is a rare disorder characterized by cerebrovascular occlusion and development of hemorrhage-prone collateral vessels. Approximately 10–12% of cases are familial, with a presumed low penetrance autosomal dominant pattern of in