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Compound heterozygosity for premature termination codon and glycine substitution mutations in the COL7A1 gene in Korean siblings with a moderately severe phenotype of recessive dystrophic epidermolysis bullosa

✍ Scribed by Kim, Jooyoung; Kim, Soo-Chan; Yasukawa, Kana; Shimizu, Hiroshi


Book ID
119292888
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
325 KB
Volume
33
Category
Article
ISSN
0923-1811

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