𝔖 Bobbio Scriptorium
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A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins

✍ Scribed by W-L. Di; R.C. Hennekam; R.E. Callard; J.I. Harper


Book ID
108670671
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
712 KB
Volume
161
Category
Article
ISSN
0007-0963

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