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Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients

✍ Scribed by Ramon Y. Birnbaum; Daniella Landau; Khalil Elbedour; Rivka Ofir; Ohad S. Birk; Rivka Carmi


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
147 KB
Volume
146A
Category
Article
ISSN
1552-4825

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✦ Synopsis


Deletion of the first pair of fibronectin type III repeats of the integrin b-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients.