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Volumn 28, Issue 1, 2001, Pages 19-20
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A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINOPHOSPHOLIPID;
CARRIER PROTEIN;
ARTICLE;
ATAXIA;
CHROMOSOME 15;
CHROMOSOME DELETION;
EPILEPSY;
FEMALE;
GENE EXPRESSION;
GENE MUTATION;
GENOME;
GENOME IMPRINTING;
HAPPY PUPPET SYNDROME;
HUMAN;
MENTAL DEFICIENCY;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
ADENOSINE TRIPHOSPHATASES;
AMINO ACID SEQUENCE;
ANGELMAN SYNDROME;
CARRIER PROTEINS;
CHROMOSOMES, HUMAN, PAIR 15;
FEMALE;
GENOMIC IMPRINTING;
HUMANS;
MEMBRANE TRANSPORT PROTEINS;
MOLECULAR SEQUENCE DATA;
MUTATION;
SEQUENCE DELETION;
SEQUENCE HOMOLOGY, AMINO ACID;
SEX FACTORS;
ATAXIA;
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EID: 0035039122
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/88209 Document Type: Article |
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Times cited : (132)
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References (15)
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