Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism.

Human mutation

Volumn 19, Issue 3, 2002, Pages 308-

  Mangino, M ^a   Flex, E ^a   Digilio, M C ^a   Giannotti, A ^a   Dallapiccola, B ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN; CARRIER PROTEIN; NOGGIN PROTEIN; PROLINE; PROTEIN; SERINE;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CHROMOSOME 17; CONGENITAL MALFORMATION; DRUG ANTAGONISM; FEMALE; FINGER JOINT; GENETICS; HAPLOTYPE; HUMAN; ITALY; MALE; MOLECULAR GENETICS; MUTATION; PROTEIN SECONDARY STRUCTURE; TOE JOINT;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; FINGER JOINT; HAPLOTYPES; HUMANS; ITALY; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PROLINE; PROTEIN STRUCTURE, SECONDARY; PROTEINS; SERINE; TOE JOINT;

MLCS; MLOWN;

EID: 0036514147     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9016     Document Type: Article

References (0)