The de novo Q167K mutation in the POU1F1 gene leads to combined pituitary hormone deficiency in an Italian patient.
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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 mouseThe role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency.
P2860
The de novo Q167K mutation in the POU1F1 gene leads to combined pituitary hormone deficiency in an Italian patient.
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2003 nî lūn-bûn
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name
The de novo Q167K mutation in ...... iciency in an Italian patient.
@en
The de novo Q167K mutation in ...... iciency in an Italian patient.
@nl
type
label
The de novo Q167K mutation in ...... iciency in an Italian patient.
@en
The de novo Q167K mutation in ...... iciency in an Italian patient.
@nl
prefLabel
The de novo Q167K mutation in ...... iciency in an Italian patient.
@en
The de novo Q167K mutation in ...... iciency in an Italian patient.
@nl
P2093
P2860
P1433
P1476
The de novo Q167K mutation in ...... iciency in an Italian patient.
@en
P2093
Amelia Morrone
Elisabetta Pasquini
Enrico Zammarchi
Giovanni Maria Poggi
Ivana Pela
Maria Alice Donati
Sabrina Malvagia
P2860
P304
P356
10.1203/01.PDR.0000084113.41375.1E
P407
P577
2003-08-06T00:00:00Z
P6179
1010577903