The human homologue of the murine Llglh gene (LLGL) maps within the Smith-Magenis syndrome region in 17p11.2

Cytogenetics and Cell Genetics

Volumn 72, Issue 1, 1996, Pages 78-82

  Koyama, K ^a   Fukushima, Y ^b,f   Inazawa, J ^c   Tomotsune, D ^d   Takahashi, N ^d,g   Nakamura, Y ^a,e  

^a CANCER INSTITUTE   (Japan)

^b SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^c KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^d OSAKA UNIVERSITY   (Japan)

^e THE UNIVERSITY OF TOKYO   (Japan)

^f SHINSHU UNIVERSITY   (Japan)

^g NARA INSTITUTE OF SCIENCE AND TECHNOLOGY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 17P; GENE LOCATION; HUMAN; HUMAN CELL; MOUSE; MOUSE MUTANT; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; CYTOSKELETAL PROTEINS; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; MICE; MOLECULAR SEQUENCE DATA; PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, NUCLEIC ACID; SYNDROME;

MURINAE;

EID: 0030067218     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134167     Document Type: Article

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