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- DOI: 10.1086/375454
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Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport
Kolehmainen J, Black, GCM, Saarinen A, Chandler K, Träskelin A-L, Perveen, R, Kivitie-Kallio S, Norio R, Warburg M, Fryns J-P, de la Chapelle A , Lehesjoki A-E
Am J Hum Genet. 2003;72:1359-1370.
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Full-text held externally
- DOI: 10.1086/375454
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Volume:
72
Start page:
1359
End page:
1370
Pagination:
1359-1370
Digital Object Identifier:
10.1086/375454
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Active
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Academic department(s):
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Manchester eScholar ID:
uk-ac-man-scw:1d6361
Created:
28th August, 2009, 23:35:48
Last modified:
15th April, 2014, 13:07:35