Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation-Reference-Cited by-同舟云学术

Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation

Published:2014-01 Issue:1 Volume:94 Page:11-22
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Dusi Sabrina,Valletta Lorella,Haack Tobias B.,Tsuchiya Yugo,Venco Paola,Pasqualato Sebastiano,Goffrini Paola,Tigano Marco,Demchenko Nikita,Wieland Thomas,Schwarzmayr Thomas,Strom Tim M.,Invernizzi Federica,Garavaglia Barbara,Gregory Allison,Sanford Lynn,Hamada Jeffrey,Bettencourt Conceição,Houlden Henry,Chiapparini Luisa,Zorzi Giovanna,Kurian Manju A.,Nardocci Nardo,Prokisch Holger,Hayflick Susan,Gout Ivan,Tiranti Valeria

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

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4. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron;Morgan;Nat. Genet.,2006

5. Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA);Kruer;Ann. Neurol.,2010

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