(Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I

CONTEXT: Pseudohypoparathyroidism type I (PHP-I) is divided into PHP-Ia with Albright hereditary osteodystrophy and PHP-Ib, which usually shows no Albright hereditary osteodystrophy features. Although PHP-Ia and PHP-Ib are typically caused by genetic defects involving α subunit of the stimulatory G...

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Bibliografiska uppgifter
I publikationen:J Endocr Soc
Huvudupphovsmän: Sano, Shinichiro, Nakamura, Akie, Matsubara, Keiko, Nagasaki, Keisuke, Fukami, Maki, Kagami, Masayo, Ogata, Tsutomu
Materialtyp: Artigo
Språk:Inglês
Publicerad: Endocrine Society 2017
Ämnen:
Clinical Research Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5779104/
https://ncbi.nlm.nih.gov/pubmed/29379892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2017-00293
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