Skip Navigation

Corrigendum for Rivolta et al., Hum. Mol. Genet. 11 (10) 1219-1227.
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (12)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Rivolta, C.
Right arrow Articles by Dryja, T. P.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Rivolta, C.
Right arrow Articles by Dryja, T. P.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2003, Vol. 12, No. 5 583-584
© 2003 Oxford University Press

Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns

Carlo Rivolta, Dror Sharon, Margaret M. DeAngelis and Thaddeus P. Dryja

Human Molecular Genetics 11, 1219–1227 (2002)

The first 10% of the full text of this article appears below.

An error has been found on page 1224 of this article, concerning the calculation of the frequency of heterozygous, unaffected carriers of recessive alleles causing retinitis pigmentosa. Specifically, the allele frequency was erroneously used as the measure of carrier frequency.

The following page shows the corrected version of page 1224 and Figure 2.

Female carriers of mutations in X-linked RP genes are all mosaics because of differential X chromosome inactivation (Lyonization). They usually have fundus features and/or electroretinographic . . . [Full Text of this Article]

NUMEROUS GENES IMPLY NUMEROUS CARRIERS


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?