Search results - ORA - Oxford University Research Archive

1 - 5 of 5

1

Journal article

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates

Belaya, K, Finlayson, S, Slater, CR, et al.
2012-07-13

2

Journal article

Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome.

Belaya, K, Finlayson, S, Cossins, J, et al.
2012-12-05

3

Conference

The spectrum of mutations that underlie the DOK7 neuromuscular junction synaptopathy, and the patient response to treatment

Beeson, D, Cossins, J, Maxwell, S, et al.
2012-03-05

4

Conference

FAST CHANNEL CONGENITAL MYASTHENIA: REVIEW OF 12 CASES AND TREATMENT CHALLENGES

Finlayson, S, Webster, R, Beeson, D, et al.
2012-11-05

5

Journal article

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

Belaya, K, Finlayson, S, Slater, CR, et al.
2012-07-05

TO TOP