Molecular basis of the brindled mouse mutant (Mo(br)): A murine model of Menkes disease

Human Molecular Genetics

Volumn 6, Issue 7, 1997, Pages 1037-1042

  Grimes, Andrew ^a   Hearn, Catherine J ^a   Lockhart, Paul ^a   Newgreen, Don F ^a   Mercer, Julian F B ^a  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATASE (CALCIUM); COPPER;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COMPARATIVE STUDY; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; COPPER DEFICIENCY; COPPER METABOLISM; GENE MUTATION; HYPOPIGMENTATION; IMMUNOBLOTTING; KIDNEY; LIVER; MENKES SYNDROME; MOUSE; MOUSE MUTANT; NONHUMAN; PRIORITY JOURNAL;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; BLOTTING, WESTERN; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CONSERVED SEQUENCE; HUMANS; KIDNEY; KIDNEY TUBULES, DISTAL; KIDNEY TUBULES, PROXIMAL; MENKES KINKY HAIR SYNDROME; MICE; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MUTATION; RECOMBINANT FUSION PROTEINS; SEQUENCE DELETION;

ANIMALIA; MURINAE;

EID: 0030752983     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.7.1037     Document Type: Article

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