𝔖 Bobbio Scriptorium
✦   LIBER   ✦

P3.21 A missense mutation in Mitofusin 2 causing early onset, progressive, axonal polyneuropathy (CMT2), optic atrophy and developmental delay in a child

✍ Scribed by G.P. Hewawitharana; T. Antoniadi; C. Faulkner; M. Williams; J. Rankin; A. Majumdar


Book ID
116795097
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
47 KB
Volume
21
Category
Article
ISSN
0960-8966

No coin nor oath required. For personal study only.