BibTex format
@inproceedings{Stutzmann:2009,
author = {Stutzmann, F and Ghoussaini, M and Couturier, C and Marchand, M and Vatin, V and Corset, L and Lecoeur, C and Balkau, B and Horber, F and Driscoll, DJ and Goldstone, AP and Weill, J and Michaud, JL and Meyre, D and Froguel, P},
pages = {S104--S104},
publisher = {SPRINGER},
title = {Loss-of-function mutations in SIM1 cause a specific form of Prader-Willi-like syndrome},
url = {https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000269262400239&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb},
year = {2009}
}
RIS format (EndNote, RefMan)
TY - CPAPER
AU - Stutzmann,F
AU - Ghoussaini,M
AU - Couturier,C
AU - Marchand,M
AU - Vatin,V
AU - Corset,L
AU - Lecoeur,C
AU - Balkau,B
AU - Horber,F
AU - Driscoll,DJ
AU - Goldstone,AP
AU - Weill,J
AU - Michaud,JL
AU - Meyre,D
AU - Froguel,P
EP - 104
PB - SPRINGER
PY - 2009///
SN - 0012-186X
SP - 104
TI - Loss-of-function mutations in SIM1 cause a specific form of Prader-Willi-like syndrome
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000269262400239&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
ER -
