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  1. Abc7 a.k.a. Abcb7 is a protein.
  2. Abc7 a.k.a. ATP-binding cassette, sub-family B (MDR/TAP), member 7 is a gene.
    • also known as Anemia, sideroblastic, with spinocerebellar ataxia; ATP-binding cassette 7; ATP-binding cassette, sub-family B, member 7

Printed dictionaries and other books with definitions for ABC7

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Google previewMolecular Biology of Metal Homeostasis and Detoxification (2006)

From Microbes to Man by Markus J. Tamás, Enrico Martinoia

Thus, ABC7 is a functional orthologue of Atm1p and plays a critical role in the maturation of Fe-S proteins. The mild hypochromic microcytic anemia in patients with XLSA/A suggests a defect in heme synthesis in developing erythroid cells.

Google previewVirtual Teams (2004)

Projects, Protocols and Processes by David Pauleen

Copying or distributing in print or electronic forms without written ABC's Virtual Team Configuration ABC7 is a multinational organization with permission of Idea Group Inc. is prohibited. The Multifaceted ...

Google previewEncyclopedia of Molecular Pharmacology

by Stefan Offermanns

transport ABCB5 ABCB6 MTABC3 Iron transport ABCB7 ABC7 Fe/S ...

Google previewSurveillance in America: An Encyclopedia of History, Politics, and the Law [2 volumes] (2016)

An Encyclopedia of History, Politics, and the Law by Pam Dixon Executive Director ...

Google previewEncyclopedia of Molecular Mechanisms of Disease (2009)

With 213 Tables by Florian Lang

DRP1 Deoxynucleotide carrier Congenital microcephaly in Amish DDP1 Deafness dystonia protein Mohr-Tranebjaerg syndrome ABC7 Iron mitochondrial export Sideroblastic anemia, ataxia Lipid milieu G4.5 Taffazin Barth syndrome ( CMP, ...

Google previewThe Mississippi Encyclopedia (2017)

by Ted Ownby, Charles Reagan Wilson, Ann J. Abadie, Odie Lindsey, James G. Thomas

ABC7 website,; ...

Google previewThe Dictionary of Genomics, Transcriptomics and Proteomics (2015)

by Guenter Kahl

ABC7 (mutations associated with Xlinked sideroblastic anemia with ataxia) and BSEP (mutations associated ...

Google previewEncyclopedia of the Neurological Sciences (2014)

The mitochondrial inner membrane iron transporter ABC7 is defective in XLSA/A.

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