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Volumn 53, Issue 3, 1998, Pages 359-364

Human DCTN1: Genomic structure and evaluation as a candidate for Alstrom syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; GENE MUTATION; GENE SEGREGATION; GENE STRUCTURE; GENOME; HUMAN; HYPERPHAGIA; NUCLEOTIDE SEQUENCE; OBESITY; PRIORITY JOURNAL; RETINA DEGENERATION; SYNDROME;

EID: 0032213761     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5542     Document Type: Article
Times cited : (14)

References (18)
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    • Alström C. H., Hallgren B., Nilsson L. B., Asander H. Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness. A specific syndrome (not hitherto described) distinct from Laurence-Moon-Biedl syndrome. A clinical endocrinological and genetic examination based on a large pedigree. Acta Psychiatr. Neurol. Scand. 1959;1-35.
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    • Dynactin, a conserved, ubiquitously expressed component of an activator of vesicle motility mediated by cytoplasmic dynein
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  • 11
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    • Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families
    • Marshall J. D., Ludman M. D., Shea S. E., Salisbury S. R., Willi S. M., LaRoche R. G., Nishina P. M. Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families. Am. J. Med. Genet. 73:1997;150-161.
    • (1997) Am. J. Med. Genet. , vol.73 , pp. 150-161
    • Marshall, J.D.1    Ludman, M.D.2    Shea, S.E.3    Salisbury, S.R.4    Willi, S.M.5    LaRoche, R.G.6    Nishina, P.M.7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.