(Q44383827)

2 December 2017

title

A novel mutation of the leptin gene in an Indian patient (English)

1 reference

2 December 2017

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

S Thakur

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A Kumar

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

S Dubey

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A N C Peters

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A Singhal

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

publication date

5 December 2013

1 reference

2 December 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

86

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

391-393

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

Congenital leptin deficiency is associated with severe early-onset obesity in humans

10 June 2020

cites work

1 reference

High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families.

21 January 2018

1 reference

Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy

21 January 2018

1 reference

Leptin deficiency and leptin gene mutations in obese children from Pakistan

21 January 2018

1 reference

Leptin replacement improves cognitive development

21 January 2018

1 reference

A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient.

21 January 2018

1 reference

A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12289

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24304187%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference