Keyword Connections

kmt2b

Journals

1

1 parkinsonism & related disorders

Research Groups

0

No Research Group Connected

Bibliographies

3

1 De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient.

2 Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia.

3 Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia.