Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects-Reference-Cited by-同舟云学术

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Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects

Published:2008-07-09 Issue:19 Volume:17 Page:3075-3083
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Yanagi T.,Akiyama M.,Nishihara H.,Sakai K.,Nishie W.,Tanaka S.,Shimizu H.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/19/3075/7072066/ddn204.pdf

Reference34 articles.

1. Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer

2. Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis

3. Harlequin ichthyosis and other autosomal recessive congenital ichthyoses: The underlying genetic defects and pathomechanisms

4. Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

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