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Output details

1 - Clinical Medicine

University College London

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Article title

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).

Type

D - Journal article

DOI

10.1093/hmg/dds194

Title of journal

Hum Mol Genet

Article number

Volume number

Issue number

First page of article

3647

ISSN of journal

0964-6906

Year of publication

2012

URL

Number of additional authors

Additional information

Interdisciplinary

Cross-referral requested

Research group

None

Citation count

Proposed double-weighted

Double-weighted statement

Reserve for a double-weighted output

Non-English

English abstract