Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency

S. Nouioua; D. Cheillan; S. Zaouidi; G.S. Salomons; N. Amedjout; F. Kessaci; N. Boulandour; T. Hamadouche; M. Tazir

doi:https://doi.org/10.1016/j.nmd.2013.04.011

Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency

S. Nouioua, D. Cheillan, S. Zaouidi, G.S. Salomons, N. Amedjout, F. Kessaci, N. Boulandour, T. Hamadouche, M. Tazir

Laboratory Medicine (VUmc)

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

28 Citations (Scopus)

Original language	English
Pages (from-to)	670-674
Journal	Neuromuscular disorders
Volume	23
Issue number	8
DOIs	https://doi.org/10.1016/j.nmd.2013.04.011
Publication status	Published - 2013

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https://doi.org/10.1016/j.nmd.2013.04.011

Cite this

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title = "Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency",

author = "S. Nouioua and D. Cheillan and S. Zaouidi and G.S. Salomons and N. Amedjout and F. Kessaci and N. Boulandour and T. Hamadouche and M. Tazir",

year = "2013",

doi = "https://doi.org/10.1016/j.nmd.2013.04.011",

language = "English",

volume = "23",

pages = "670--674",

journal = "Neuromuscular disorders",

issn = "0960-8966",

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T1 - Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency

AU - Nouioua, S.

AU - Cheillan, D.

AU - Zaouidi, S.

AU - Salomons, G.S.

AU - Amedjout, N.

AU - Kessaci, F.

AU - Boulandour, N.

AU - Hamadouche, T.

AU - Tazir, M.

PY - 2013

Y1 - 2013

U2 - https://doi.org/10.1016/j.nmd.2013.04.011

DO - https://doi.org/10.1016/j.nmd.2013.04.011

M3 - Article

C2 - 23770102

SN - 0960-8966

VL - 23

SP - 670

EP - 674

JO - Neuromuscular disorders

JF - Neuromuscular disorders

IS - 8

ER -