Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency. [electronic resource]

By: Contributor(s): Producer: 20170111Description: 373-81 p. digitalISSN:
  • 2190-3883
Subject(s): Online resources: In: Journal of applied genetics vol. 57
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Publication Type: Journal Article

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