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ECEL1 mutation causes fetal arthrogryposis multiplex congenita
Dohrn, N., Le, V.Q., Petersen, A., Skovbo, P., Pedersen, I.S., Ernst, A., Krarup, H., Petersen, M.B.Volume:
167
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.37018
Date:
April, 2015
File:
PDF, 5.58 MB
english, 2015