P57 IGHMBP2 mutations cause recessive axonal neuropathy: Genetic and functional characterisation in seven families

Journal article

Peer reviewed

E Cottenie, A Kochanski, A Jordanova, J Baets, V. Milic Rasic, R Quinlivan, M Lunn, M.G Hanna, S Zuchner, M Harms, …

Neuromuscular disorders : NMD, Vol.24, pp.S22-S22

2014-03

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Title: P57 IGHMBP2 mutations cause recessive axonal neuropathy: Genetic and functional characterisation in seven families
Creators: E Cottenie
A Kochanski
A Jordanova
J Baets
V. Milic Rasic
R Quinlivan
M Lunn
M.G Hanna
S Zuchner
M Harms
B Choi
M.M Reilly
H Houlden
Publication Details: Neuromuscular disorders : NMD, Vol.24, pp.S22-S22
Academic Unit: Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
Language: English
Resource Type: Journal article
Record Identifier: 991031600006402976