An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

TS Khurshid; Johnny Moore; AB Page; J Darling; DJ Atherton; MA Van Steensel; CS Munro; FJ Amith; JA McGrath

An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

TS Khurshid, Johnny Moore, AB Page, J Darling, DJ Atherton, MA Van Steensel, CS Munro, FJ Amith, JA McGrath

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

Original language	English
Pages (from-to)	2395-2409
Journal	Human Molecular Genetics
Volume	12
Issue number	18
Publication status	Published (in print/issue) - 2003

Cite this

@article{9460a38608ad41b3906089368435f683,

title = "An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome",

author = "TS Khurshid and Johnny Moore and AB Page and J Darling and DJ Atherton and {Van Steensel}, MA and CS Munro and FJ Amith and JA McGrath",

year = "2003",

language = "English",

volume = "12",

pages = "2395--2409",

journal = "Human Molecular Genetics",

issn = "1460-2083",

publisher = "Oxford University Press",

number = "18",

}

TY - JOUR

T1 - An unusual N-terminal deletion of the laminin {alpha}3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome

AU - Khurshid, TS

AU - Moore, Johnny

AU - Page, AB

AU - Darling, J

AU - Atherton, DJ

AU - Van Steensel, MA

AU - Munro, CS

AU - Amith, FJ

AU - McGrath, JA

PY - 2003

Y1 - 2003

M3 - Article

SN - 1460-2083

VL - 12

SP - 2395

EP - 2409

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 18

ER -