New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype.
about
Associations of POU1F1 gene polymorphisms and protein structure changes with growth traits and blood metabolites in two Iranian sheep breeds.Genetic regulation of pituitary gland development in human and mouseIdentification of Candidate Genes for Reactivity in Guzerat (Bos indicus) Cattle: A Genome-Wide Association Study.The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.
P2860
New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
New N-terminal located mutatio ...... ciency and variable phenotype.
@en
type
label
New N-terminal located mutatio ...... ciency and variable phenotype.
@en
prefLabel
New N-terminal located mutatio ...... ciency and variable phenotype.
@en
P2093
P1476
New N-terminal located mutatio ...... ciency and variable phenotype.
@en
P2093
Amélie Besson
Andrée Eblé
Primus E Mullis
Roland W Pfäffle
Sabina Gallati
Souzan Salemi
P304
P356
10.1016/S1096-6374(03)00015-7
P577
2003-10-01T00:00:00Z