Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing

Published 2013 View Full Article

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Title
Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing
Authors
Keywords
-
Journal
Hormone Research in Paediatrics
Volume 79, Issue 6, Pages 379-386
Publisher
S. Karger AG
Online
2013-05-06
DOI
10.1159/000350013

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