Late diagnosis of a truncating WISP3...

Molecular Case Studies 2018 / 02 Vol. 4; Iss. 1

Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia

Alawbathani, Salem, Kawalia, Amit, Karakaya, Mert, Altmüller, Janine, Nürnberg, Peter, Cirak, Sebahattin
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Volume:
4
Language:
english
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a002139
Date:
February, 2018
File:
PDF, 2.26 MB
english, 2018
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