Menkes disease mutations and response to early copper histidine treatment

Nature Genetics

Volumn 13, Issue 1, 1996, Pages 21-22

  Kaler, Stephen G ^a,b  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ATP7A PROTEIN, HUMAN; CARRIER PROTEIN; CATION TRANSPORT PROTEIN; COPPER; DRUG DERIVATIVE; HISTIDINE; HISTIDINE COPPER; HYBRID PROTEIN; ORGANOMETALLIC COMPOUND;

EXON; GENETICS; HUMAN; LETTER; MENKES SYNDROME; MUTATION; POLYMERASE CHAIN REACTION;

ADENOSINE TRIPHOSPHATASES; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; COPPER; EXONS; HISTIDINE; HUMANS; MENKES KINKY HAIR SYNDROME; MUTATION; ORGANOMETALLIC COMPOUNDS; POLYMERASE CHAIN REACTION; RECOMBINANT FUSION PROTEINS;

EID: 0030138462     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0596-21     Document Type: Article

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