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Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome

✍ Scribed by E. Sprecher; A. Tesfaye-Kedjela; P. Ratajczak; R. Bergman; G. Richard


Book ID
108693080
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
259 KB
Volume
29
Category
Article
ISSN
0307-6938

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