WNT1 mutation with recessive osteogenesis imperfecta and...

Journal of Medical Genetics 2013 / 07 Vol. 50; Iss. 7

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Faqeih, E., Shaheen, R., Alkuraya, F. S.
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Volume:
50
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2013-101750
Date:
July, 2013
File:
PDF, 159 KB
english, 2013
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