A Mutational Hot Spot in the Prop-1 Gene in Russian Children with Combined Pituitary Hormone Deficiency

Pituitary

Volumn 1, Issue 1, 1998, Pages 45-49

  Fofanova, Olga V ^a   Takamura, Noboru ^c   Kinoshita, Ei Ichi ^d   Parks, John S ^e   Brown, Milton R ^e   Peterkova, Valentina A ^a   Evgrafov, Oleg V ^b   Goncharov, Nikolai P ^b   Bulatov, Alexander A ^b   Dedov, Ivan I ^b   Yamashita, Shunichi ^c,f  

^a N N BLOKHIN NATIONAL MEDICAL RESEARCH CENTER OF ONCOLOGY   (Russian Federation)

^b ENDOCRINOLOGY RESEARCH CENTRE   (Russian Federation)

^c NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d NAGASAKI UNIVERSITY   (Japan)

^e EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f NONE   (Japan)

Author keywords

2 base pair deletion GA296; Combined pituitary hormone deficiency (CPHD); Prophet of Pit 1 (Prop 1); Russia

Indexed keywords

HOMEODOMAIN PROTEIN; HUMAN GROWTH HORMONE; HYPOPHYSIS HORMONE; PROLACTIN; PROPHET OF PIT 1 PROTEIN; PROPHET OF PIT-1 PROTEIN; THYROTROPIN;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CHILD; FEMALE; GENE DELETION; GENETICS; HUMAN; MALE; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RECESSIVE GENE; RUSSIAN FEDERATION; SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; HOMEODOMAIN PROTEINS; HUMAN GROWTH HORMONE; HUMANS; MALE; MICE; MUTATION; PEDIGREE; PITUITARY HORMONES; PROLACTIN; RUSSIA; SEQUENCE DELETION; SYNDROME; THYROTROPIN;

EID: 0032034425     PISSN: 1386341X     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1009918924945     Document Type: Article

References (20)

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