Identification of a novel mutation in a patient with pseudohypoparathyroidism type Ia
Pseudohypoparathyroidism type Ia (PHP Ia) is a disorder characterized by multiform hormonal resistance including parathyroid hormone (PTH) resistance and Albright hereditary osteodystrophy (AHO). It is caused by heterozygous inactivating mutations within the Gs alpha-encoding GNAS exons. A 9-year-ol...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Korean Pediatric Society
2014-05-01
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Series: | Korean Journal of Pediatrics |
Subjects: | |
Online Access: | http://kjp.or.kr/upload/pdf/kjped-57-240.pdf |