Intragenic deletions at Atp7a in mouse models for Menkes disease

Genomics

Volumn 74, Issue 2, 2001, Pages 155-162

  Cunliffe, Pamela ^a   Reed, Vivienne ^b   Boyd, Yvonne ^c  

^a ST MARY S HOSPITAL   (United Kingdom)

^b MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

^c INSTITUTE FOR ANIMAL HEALTH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATASE ATP 7 A; COPPER; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CLASSIFICATION; EXON; GENE DELETION; MALE; MENKES SYNDROME; MOLECULAR GENETICS; MOUSE; NONHUMAN; NONSENSE MUTATION; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0035366410     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2001.6529     Document Type: Article

References (47)

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32. Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1D69Q mutation
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45. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis