A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient [4]

Clinical Genetics

Volumn 56, Issue 6, 1999, Pages 469-470

  Lucotte, G ^a   Semonin, O ^a   Lutz, P ^a  

^a Centre de Neurogenetique Moleculaire   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SECRETORY PROTEIN;

CASE REPORT; DEVELOPMENTAL GENETICS; GENE DELETION; HETEROZYGOSITY; HUMAN; HUMAN CELL; LETTER; NUCLEOTIDE SEQUENCE; OSSIFYING MYOSITIS; PRIORITY JOURNAL;

BASE SEQUENCE; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; ELECTROPHORESIS, AGAR GEL; GENE DELETION; HETEROZYGOTE; HUMANS; MOLECULAR SEQUENCE DATA; MYOSITIS OSSIFICANS; POLYMERASE CHAIN REACTION; PROTEINS;

EID: 0033428271     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.560613.x     Document Type: Letter

References (10)