Glial Cell Missing Homolog 2 Mutation Causing Severe Hypoparathyroidism: Report of Two Cases With Novel Mutations.

Singhania, Pankaj; Ghosh, Arunava; Das, Debaditya; Bhattacharjee, Rana; Roy, Ajitesh; Chowdhury, Subhankar

Singhania, Pankaj; Ghosh, Arunava; Das, Debaditya; Bhattacharjee, Rana; Roy, Ajitesh; Chowdhury, Subhankar.

Afiliação

Singhania P; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, Kolkata, India.
Ghosh A; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, Kolkata, India.
Das D; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, Kolkata, India.
Bhattacharjee R; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, Kolkata, India.
Roy A; Vivekananda Institute of Medical Sciences, Kolkata, India.
Chowdhury S; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, Kolkata, India.

J Endocr Soc ; 7(1): bvac166, 2022 Nov 17.

Article em En | MEDLINE | ID: mdl-36405867

Palavras-chave

CaSR; GCM2; hypocalcemia; idiopathic; parathyroid

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Endocr Soc Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia País de publicação: Estados Unidos

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