Novel LRRK2 mutation in the Roc domain in an Western Australian family with autosomal dominant late-onset Parkinson's disease (LOPD)

F. L. Mastaglia, Y. Huang, G. Halliday, D. B. Rowe, C. M. Sue

Research output: Contribution to journal › Meeting abstract

Cite this

@article{0171fb1c5a894780aa629a2bd49e8ff8,

title = "Novel LRRK2 mutation in the Roc domain in an Western Australian family with autosomal dominant late-onset Parkinson's disease (LOPD)",

author = "Mastaglia, {F. L.} and Y. Huang and G. Halliday and Rowe, {D. B.} and Sue, {C. M.}",

year = "2007",

language = "English",

volume = "22",

pages = "729--729",

journal = "Movement Disorders",

issn = "0885-3185",

publisher = "Lippincott Williams & Wilkins",

number = "Suppl. 16",

}

TY - JOUR

T1 - Novel LRRK2 mutation in the Roc domain in an Western Australian family with autosomal dominant late-onset Parkinson's disease (LOPD)

AU - Mastaglia, F. L.

AU - Huang, Y.

AU - Halliday, G.

AU - Rowe, D. B.

AU - Sue, C. M.

PY - 2007

Y1 - 2007

M3 - Meeting abstract

SN - 0885-3185

VL - 22

SP - 729

EP - 729

JO - Movement Disorders

JF - Movement Disorders

IS - Suppl. 16

ER -