Carregant...

(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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: Sano, Shinichiro, Nakamura, Akie, Matsubara, Keiko, Nagasaki, Keisuke, Fukami, Maki, Kagami, Masayo, Ogata, Tsutomu
Format: Artigo
Idioma:Inglês
Publicat: Endocrine Society 2017
Matèries:
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!