Cap disease caused by heterozygous deletion of the ß-tropomyosin gene TPM2

Vilma-Lotta Lehtokari; Chantal Ceuterick-de Groote; Peter de Jonghe; Minttu Marjaana Marttila; Nigel G Laing; Katarina Pelin; Carina Wallgren-Pettersson; Minttu Martiila

Cap disease caused by heterozygous deletion of the ß-tropomyosin gene TPM2

Vilma-Lotta Lehtokari, Chantal Ceuterick-de Groote, Peter de Jonghe, Minttu Marjaana Marttila, Nigel G Laing, Katarina Pelin, Carina Wallgren-Pettersson, Minttu Martiila

Avdelningen för medicinsk genetik och klinisk genetik

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Tidskrift	Neuromuscular Disorders
Volym	17
Nummer	6
Sidor (från-till)	433-442
Antal sidor	10
ISSN	0960-8966
Status	Publicerad - 2007
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Citera det här

@article{2670d1a2f2a44ba085628a57cc88e812,

title = "Cap disease caused by heterozygous deletion of the {\ss}-tropomyosin gene TPM2",

author = "Vilma-Lotta Lehtokari and \{Ceuterick-de Groote\}, Chantal and \{de Jonghe\}, Peter and Marttila, \{Minttu Marjaana\} and Laing, \{Nigel G\} and Katarina Pelin and Carina Wallgren-Pettersson and Minttu Martiila",

year = "2007",

language = "English",

volume = "17",

pages = "433--442",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Ltd. ",

number = "6",

}

TY - JOUR

T1 - Cap disease caused by heterozygous deletion of the ß-tropomyosin gene TPM2

AU - Lehtokari, Vilma-Lotta

AU - Ceuterick-de Groote, Chantal

AU - de Jonghe, Peter

AU - Marttila, Minttu Marjaana

AU - Laing, Nigel G

AU - Pelin, Katarina

AU - Wallgren-Pettersson, Carina

AU - Martiila, Minttu

PY - 2007

Y1 - 2007

M3 - Article

SN - 0960-8966

VL - 17

SP - 433

EP - 442

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 6

ER -