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

External organisation

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

33 Citations (Scopus)

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

Research programs

EMC 05-04-21-02-00
EMC MM-01-54-01
EMC MM-04-44-02

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 -