Genetic basis of hyperlysinemia

SM Houten; H te Brinke; S Denis; JPN Ruiter; AC Knegt; Hans Klerk; P Augoustides-Savvopoulou; J Haberle; MR Baumgartner; T Coskun; J Zschocke; JO Sass; BT Poll-The; RJA Wanders; M (Mercedes) Duran

doi:10.1186/1750-1172-8-57

Genetic basis of hyperlysinemia

SM Houten
, H te Brinke
, S Denis
, JPN Ruiter
, AC Knegt
, Hans Klerk
, P Augoustides-Savvopoulou
, J Haberle
, MR Baumgartner
, T Coskun
, J Zschocke
, JO Sass
, BT Poll-The
, RJA Wanders
, M (Mercedes) Duran

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

50 Citations (Scopus)

42 Downloads (Pure)

Original language	Undefined/Unknown
Journal	Orphanet Journal of Rare Diseases
Volume	8
DOIs	https://doi.org/10.1186/1750-1172-8-57
Publication status	Published - 2013

Research programs

EMC MM-01-54-01

Access to Document

10.1186/1750-1172-8-57

REPUB_61443_OA.pdfFinal published version, 441 KB

http://hdl.handle.net/1765/61443

Cite this

@article{b72e1c0031be4e8e847bef8aabe1776a,

title = "Genetic basis of hyperlysinemia",

author = "SM Houten and \{te Brinke\}, H and S Denis and JPN Ruiter and AC Knegt and Hans Klerk and P Augoustides-Savvopoulou and J Haberle and MR Baumgartner and T Coskun and J Zschocke and JO Sass and BT Poll-The and RJA Wanders and Duran, \{M (Mercedes)\}",

year = "2013",

doi = "10.1186/1750-1172-8-57",

language = "Undefined/Unknown",

volume = "8",

journal = "Orphanet Journal of Rare Diseases",

issn = "1750-1172",

publisher = "BioMed Central Ltd.",

}

TY - JOUR

T1 - Genetic basis of hyperlysinemia

AU - Houten, SM

AU - te Brinke, H

AU - Denis, S

AU - Ruiter, JPN

AU - Knegt, AC

AU - Klerk, Hans

AU - Augoustides-Savvopoulou, P

AU - Haberle, J

AU - Baumgartner, MR

AU - Coskun, T

AU - Zschocke, J

AU - Sass, JO

AU - Poll-The, BT

AU - Wanders, RJA

AU - Duran, M (Mercedes)

PY - 2013

Y1 - 2013

U2 - 10.1186/1750-1172-8-57

DO - 10.1186/1750-1172-8-57

M3 - Article

C2 - 23570448

SN - 1750-1172

VL - 8

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

ER -