Novel PRG4 mutations underlie CACP in Saudi families.

Human mutation

Volumn 27, Issue 2, 2006, Pages 213-

  Alazami, Anas M ^a   Al Mayouf, Sulaiman M ^a   Wyngaard, Carol Ann ^a   Meyer, Brian ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

PRG4 PROTEIN, HUMAN; PROTEOGLYCAN;

ALLELE; ARTICLE; BONE DISEASE; CHILD; FAMILY HEALTH; FEMALE; GENETICS; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; MUTATION; NEUROPATHIC JOINT DISEASE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; SAUDI ARABIA; SYNDROME;

ABNORMALITIES, MULTIPLE; ALLELES; ARTHROPATHY, NEUROGENIC; BONE DISEASES; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HUMANS; INFANT; MALE; MUTATION; PROTEOGLYCANS; SAUDI ARABIA; SYNDROME;

EID: 33745939347     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9399     Document Type: Article

References (0)