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Comment
. 2013 Jul;50(7):491-2.
doi: 10.1136/jmedgenet-2013-101750. Epub 2013 May 24.

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Eissa Faqeih, Ranad Shaheen, Fowzan S Alkuraya
Comment

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype

Eissa Faqeih et al. J Med Genet. 2013 Jul.
No abstract available

Keywords: Academic medicine.

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