Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)

L Baumber, S Patel, E Kinning, P Critchley, A H Nemeth, K Talbot, E R Maher, R C Trembath

Research output: Contribution to journal › Meeting abstract

Original language	English
Article number	2.10
Pages (from-to)	S82 - S82
Journal	Journal of Medical Genetics
Volume	44
Publication status	Published - 2007
Event	British Human Genetics Conference - York, ENGLAND Duration: 17 Sept 2007 → 20 Sept 2007

Cite this

@article{6d2c0439aafa4e8d8c38b88b8b627283,

title = "Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)",

author = "L Baumber and S Patel and E Kinning and P Critchley and Nemeth, {A H} and K Talbot and Maher, {E R} and Trembath, {R C}",

year = "2007",

language = "English",

volume = "44",

pages = "S82 -- S82",

journal = "Journal of Medical Genetics",

issn = "1468-6244",

publisher = "B M J PUBLISHING GROUP",

note = "British Human Genetics Conference ; Conference date: 17-09-2007 Through 20-09-2007",

}

TY - JOUR

T1 - Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)

AU - Baumber, L

AU - Patel, S

AU - Kinning, E

AU - Critchley, P

AU - Nemeth, A H

AU - Talbot, K

AU - Maher, E R

AU - Trembath, R C

PY - 2007

Y1 - 2007

M3 - Meeting abstract

SN - 1468-6244

VL - 44

SP - S82 - S82

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

M1 - 2.10

T2 - British Human Genetics Conference

Y2 - 17 September 2007 through 20 September 2007

ER -