Molybdenum Cofactor (moco) Deficiency Type B; Clinical, Biochemical and Neuroimaging Features of Five Patients Wth Two Novel Mutations

B. Hismi; O. Unal; J. O. Sass; F. Beermann; K. Ichida; A. Dursun; H. S. Sivri; A. Tokatli; T. Coskun

Molybdenum Cofactor (moco) Deficiency Type B; Clinical, Biochemical and Neuroimaging Features of Five Patients Wth Two Novel Mutations

B. Hismi
, O. Unal
, J. O. Sass
, F. Beermann
, K. Ichida
, A. Dursun
, H. S. Sivri
, A. Tokatli
, T. Coskun

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

Original language	English
Pages (from-to)	S136-S136
Number of pages	1
Journal	Journal of Inherited Metabolic Disease
Volume	35
Publication status	Published - Sept 2012

Cite this

@article{73cded3cf05b4c47b0a5a69464afc8f3,

title = "Molybdenum Cofactor (moco) Deficiency Type B; Clinical, Biochemical and Neuroimaging Features of Five Patients Wth Two Novel Mutations",

author = "B. Hismi and O. Unal and Sass, \{J. O.\} and F. Beermann and K. Ichida and A. Dursun and Sivri, \{H. S.\} and A. Tokatli and T. Coskun",

year = "2012",

month = sep,

language = "English",

volume = "35",

pages = "S136--S136",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

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TY - JOUR

T1 - Molybdenum Cofactor (moco) Deficiency Type B; Clinical, Biochemical and Neuroimaging Features of Five Patients Wth Two Novel Mutations

AU - Hismi, B.

AU - Unal, O.

AU - Sass, J. O.

AU - Beermann, F.

AU - Ichida, K.

AU - Dursun, A.

AU - Sivri, H. S.

AU - Tokatli, A.

AU - Coskun, T.

PY - 2012/9

Y1 - 2012/9

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:000307513100475&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 0141-8955

VL - 35

SP - S136-S136

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

ER -

Molybdenum Cofactor (moco) Deficiency Type B; Clinical, Biochemical and Neuroimaging Features of Five Patients Wth Two Novel Mutations

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