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Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lefèvre syndrome: Implications for understanding the genotype/phenotype relationship

✍ Scribed by Ochiai, Toyoko; Nakano, Hajime; Rokunohe, Daiki; Akasaka, Eijiro; Toyomaki, Yuka; Mitsuhashi, Yoshihiko; Sawamura, Daisuke


Book ID
119293397
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
349 KB
Volume
53
Category
Article
ISSN
0923-1811

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