Publications: DR Azizun Nessa
Nessa A, Aziz QH, Thomas AM, Harmer SC, Tinker A, Hussain K
(
2015
)
.
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8
.
Human Molecular Genetics
vol.
24
,
(
18
)
5142
-
5153
.
Arya VB, Aziz Q, Nessa A, Tinker A, Hussain K
(
2014
)
.
Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy
.
International Journal of Pediatric Endocrinology
vol.
2014
,
(
1
)