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New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome

✍ Scribed by Fuchs-Telem, D.; Nousbeck, J.; Singer, A.; McGrath, J. A.; Sarig, O.; Sprecher, E.

Book ID: 127036051
Publisher: John Wiley and Sons
Year: 2014
Tongue: English
Weight: 1001 KB
Volume: 39
Category: Article
ISSN: 0307-6938
DOI: 10.1111/ced.12222

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