Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 10(39), p. 1349-1354, 2018
DOI: 10.1002/humu.23592
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Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1 ) in a patient with concomitant simplex and junctional epidermolysis bullosa
Journal article published in 2018 by
Hassan Vahidnezhad,
Leila Youssefian,
Amir Hossein Saeidian,
Andrew Touati,
Soheila Sotoudeh,
Ali Jazayeri,
Alyson Guy,
Patricia A. Lovell,
Lu Liu,
Ariana Kariminejad 
,
John A. McGrath,
Sirous Zeinali,
Jouni Uitto
,
John A. McGrath,
Sirous Zeinali,
Jouni Uitto
This paper was not found in any repository, but could be made available legally by the author.
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