WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype.

Journal of medical genetics

Volumn 50, Issue 7, 2013, Pages 491-492

  Faqeih, Eissa ^a   Shaheen, Ranad ^a   Alkuraya, Fowzan S ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

WNT1 PROTEIN;

BONE; CHEMICAL STRUCTURE; FEMALE; GENETICS; HUMAN; OSTEOGENESIS IMPERFECTA; PROTEIN CONFORMATION; RADIOGRAPHY;

BONE AND BONES; FEMALE; HUMANS; MODELS, MOLECULAR; OSTEOGENESIS IMPERFECTA; PROTEIN CONFORMATION; WNT1 PROTEIN;

EID: 84894327119     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2013-101750     Document Type: Note

References (0)