A new mutation of the Noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family

Genetic Counseling

Volumn 16, Issue 2, 2005, Pages 149-154

  Fontaine, K ^a   Semonin O ^a   Lagarde, J P ^b   Lenoir, G ^c   Lucotte, Gerard ^d,e  

^a Euro Sequence Gene Service   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d Center of Molecular Neurogenetics   (France)

^e Centre de Neurogenetique Moleculaire   (France)

Author keywords

Fibrodysplasia ossificans progressiva (FOP); French FOP family; Myristoylation site; Noggin (NOG) gene Mutation A95T

Indexed keywords

ADENINE; ALANINE; GUANINE; NOGGIN; NUCLEOTIDE;

AMINO ACID SEQUENCE; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE TRANSMISSION; FEMALE; FIBROUS DYSPLASIA; FRANCE; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; MYRISTYLATION; RARE DISEASE;

ADENOSINE; CARRIER PROTEINS; CHROMOSOMES, HUMAN, PAIR 17; DNA MUTATIONAL ANALYSIS; GUANINE; HALLUX VALGUS; HETEROZYGOTE DETECTION; HUMANS; INFANT, NEWBORN; MALE; MYOSITIS OSSIFICANS; PEDIGREE; PEPTIDES; SEQUENCE ANALYSIS, DNA;

EID: 22444448252     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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