Contiguous gene deletion syndrome in Xp21

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Bibliographic Details
Published inRevista de neurologiá Vol. 50; no. 3; p. 192
Main Authors Duat-Rodríguez, Anna, Gutiérrez-Solana, Luis G, García-Peñas, Juan José, Ruiz-Falcó, María Luz
Format Journal Article
LanguageSpanish
Published Spain 01.02.2010
Subjects
Adrenal Insufficiency - genetics
Adrenal Insufficiency - physiopathology
Chromosomes, Human, X - genetics
Creatine Kinase - blood
Electromyography
Gene Deletion
Genetic Diseases, X-Linked - genetics
Genetic Diseases, X-Linked - physiopathology
Glycerol Kinase - genetics
Glycerol Kinase - metabolism
Humans
Infant
Muscular Dystrophy, Duchenne - genetics
Muscular Dystrophy, Duchenne - physiopathology
Syndrome
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ObjectType-Commentary-2
ISSN:1576-6578
DOI:10.33588/rn.5003.2009701