Basal ganglia involvement in childhood: Creatine deficiency syndrome caused by guanidinoacetate methyltransferase (GAMT) deficiency

G. Haliloglu; A. Dursun; K. K. Oguz; D. Yalnyzoglu; H. Y. Aydin; S. Aysun; H. S. Sivri; T. Coskun; A. Tokatli

Basal ganglia involvement in childhood: Creatine deficiency syndrome caused by guanidinoacetate methyltransferase (GAMT) deficiency

G. Haliloglu
, A. Dursun
, K. K. Oguz
, D. Yalnyzoglu
, H. Y. Aydin
, S. Aysun
, H. S. Sivri
, T. Coskun
, A. Tokatli

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	145-145
Number of pages	1
Journal	Journal of Inherited Metabolic Disease
Volume	29
Publication status	Published - Aug 2006

Cite this

@article{fa64033e0f014a96aefa4e47796d5d0e,

title = "Basal ganglia involvement in childhood: Creatine deficiency syndrome caused by guanidinoacetate methyltransferase (GAMT) deficiency",

author = "G. Haliloglu and A. Dursun and Oguz, \{K. K.\} and D. Yalnyzoglu and Aydin, \{H. Y.\} and S. Aysun and Sivri, \{H. S.\} and T. Coskun and A. Tokatli",

year = "2006",

month = aug,

language = "English",

volume = "29",

pages = "145--145",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

}

TY - JOUR

T1 - Basal ganglia involvement in childhood

T2 - Creatine deficiency syndrome caused by guanidinoacetate methyltransferase (GAMT) deficiency

AU - Haliloglu, G.

AU - Dursun, A.

AU - Oguz, K. K.

AU - Yalnyzoglu, D.

AU - Aydin, H. Y.

AU - Aysun, S.

AU - Sivri, H. S.

AU - Coskun, T.

AU - Tokatli, A.

PY - 2006/8

Y1 - 2006/8

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:000240467100553&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 0141-8955

VL - 29

SP - 145

EP - 145

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

ER -

Basal ganglia involvement in childhood: Creatine deficiency syndrome caused by guanidinoacetate methyltransferase (GAMT) deficiency

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