A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome
- 31 July 2006
- journal article
- case report
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 155 (5) , 1067-1069
- https://doi.org/10.1111/j.1365-2133.2006.07449.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Detection of 1733insC mutations in an Asian family with Birt-Hogg-Dubé syndromeBritish Journal of Dermatology, 2005
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