Plasmolipin: Genomic structure, chromosomal localization, protein expression pattern, and putative association with bardet-biedl syndrome

Mammalian Genome

Volumn 12, Issue 12, 2001, Pages 933-937

  Hamacher, Michael ^a   Pippirs, Ulrich ^a   Köhler, Angelika ^b   Müller, Hans Werner ^a   Bosse, Frank ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

^b JUSTUS LIEBIG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; MYELIN PROTEIN; PLASMOLIPIN; UNCLASSIFIED DRUG;

ARTICLE; BARDET BIEDL SYNDROME; CHROMOSOMAL LOCALIZATION; CHROMOSOME 16Q; DYSTROPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE LOCUS; GENE MAPPING; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC ORGANIZATION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; HUMAN TISSUE; KIDNEY FAILURE; MENTAL DEFICIENCY; NUCLEOTIDE SEQUENCE; OBESITY; PHENOTYPE; POLYDACTYLY; PROTEIN EXPRESSION;

ANIMALS; BARDET-BIEDL SYNDROME; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; CRICETINAE; GENE EXPRESSION REGULATION; GENES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MEMBRANE PROTEINS; MESOCRICETUS; MICE; MULTIGENE FAMILY; NERVE TISSUE PROTEINS; ORGAN SPECIFICITY; PROTEOLIPIDS; RADIATION HYBRID MAPPING; RATS; SPECIES SPECIFICITY;

MAMMALIA;

EID: 0035172175     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00335-001-3035-5     Document Type: Article

References (35)

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