A mitochondrial tRNA val gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

IFM Coo; EA Sistermans; IJ de Wijs; Coriene Catsman - Berrevoets; HFM (Herman) Busch; Jasper Scholte; Hans Klerk; BA van Oost; HJM Smeets

A mitochondrial tRNA val gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

IFM Coo, EA Sistermans, IJ de Wijs, Coriene Catsman - Berrevoets, HFM (Herman) Busch, Jasper Scholte, Hans Klerk, BA van Oost, HJM Smeets

Research output: Contribution to journal › Article › Academic › peer-review

31 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	293-295
Number of pages	3
Journal	Neurology
Volume	50
Publication status	Published - 1998

Cite this

@article{7f5096a98a3240f78d96542a8ee50c1c,

title = "A mitochondrial tRNA val gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes",

author = "IFM Coo and EA Sistermans and {de Wijs}, IJ and {Catsman - Berrevoets}, Coriene and Busch, {HFM (Herman)} and Jasper Scholte and Hans Klerk and {van Oost}, BA and HJM Smeets",

year = "1998",

language = "Undefined/Unknown",

volume = "50",

pages = "293--295",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams & Wilkins",

}

TY - JOUR

T1 - A mitochondrial tRNA val gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

AU - Coo, IFM

AU - Sistermans, EA

AU - de Wijs, IJ

AU - Catsman - Berrevoets, Coriene

AU - Busch, HFM (Herman)

AU - Scholte, Jasper

AU - Klerk, Hans

AU - van Oost, BA

AU - Smeets, HJM

PY - 1998

Y1 - 1998

M3 - Article

SN - 0028-3878

VL - 50

SP - 293

EP - 295

JO - Neurology

JF - Neurology

ER -