Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history-Reference-Cited by-同舟云学术

Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history

Published:2011-09-20 Issue:11 Volume:32 Page:1204-1212
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Has Cristina,Castiglia Daniele,del Rio Marcela,Garcia Diez Marta,Piccinni Eugenia,Kiritsi Dimitra,Kohlhase Jürgen,Itin Peter,Martin Ludovic,Fischer Judith,Zambruno Giovanna,Bruckner-Tuderman Leena

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. Unusual molecular findings in Kindler syndrome;Arita;Br J Dermatol,2007

2. Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome;Ashton;J Invest Dermatol,2004

3. Kindler syndrome: a new mutation and new diagnostic possibilities;Burch;Arch Dermatol,2006

4. Aggressive squamous cell carcinoma in Kindler syndrome;Emanuel;SKINmed,2006

5. Neonatal diagnosis of Kindler syndrome;Fassihi;J Dermatol Sci,2005

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