(Q60021525)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Genetic developments in hypoparathyroidism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

RV Thakker

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 March 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

357

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

9261

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

974-976

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Positional cloning of the APECED gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Genetic ablation of parathyroid glands reveals another source of parathyroid hormone

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Isolation and characterization of mammalian homologs of the Drosophila gene glial cells missing

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

GATA3 haplo-insufficiency causes human HDR syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2904254-9

7 January 2021

10.1016/S0140-6736(00)04254-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11293637%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference