Point mutations in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families


Korge, B.P., Healy, E., Traupe, H., Pünter, C., Mauch, C., Hamm, H., Birch-Machin, M.A., Belgaid, C.E., Stephenson, A.M., Holmes, S.C., Darlington, S., Messenger, A.G., Rees, J.L. and Munro, C.S. (1999) Point mutations in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families [in special issue: Proceedings from the 1st International Meeting of Hair Research Societies] Experimental Dermatology, 8, (4), pp. 310-312. (doi:10.1111/j.1600-0625.1999.tb00384.x). (PMID:10439241).

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Item Type: Article
Digital Object Identifier (DOI): doi:10.1111/j.1600-0625.1999.tb00384.x
ISSNs: 0906-6705 (print)
Subjects:
Organisations: Clinical & Experimental Sciences
ePrint ID: 334278
Date :
Date Event
August 1999Published
Date Deposited: 13 Mar 2012 16:14
Last Modified: 17 Apr 2017 17:27
Further Information:Google Scholar
URI: http://eprints.soton.ac.uk/id/eprint/334278

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