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A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein

✍ Scribed by Gottfried, I.


Book ID
124066352
Publisher
Oxford University Press
Year
2002
Tongue
English
Weight
1004 KB
Volume
11
Category
Article
ISSN
0964-6906

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