Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria

Translated title of the contribution: Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria

M. Veiga-da-Cunha, N.M. Verhoeven - Duif, T.J. de Koning, M. Duran, B. Dorland, E. van Schaftingen

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

Translated title of the contribution	Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria
Original language	Undefined/Unknown
Pages (from-to)	961-966
Number of pages	6
Journal	Journal of Inherited Metabolic Disease
Volume	36
Issue number	6
Publication status	Published - 2013

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title = "Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria",

author = "M. Veiga-da-Cunha and \{Verhoeven - Duif\}, N.M. and \{de Koning\}, T.J. and M. Duran and B. Dorland and \{van Schaftingen\}, E.",

year = "2013",

language = "Undefined/Unknown",

volume = "36",

pages = "961--966",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "6",

}

TY - JOUR

T1 - Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria

AU - Veiga-da-Cunha, M.

AU - Verhoeven - Duif, N.M.

AU - de Koning, T.J.

AU - Duran, M.

AU - Dorland, B.

AU - van Schaftingen, E.

PY - 2013

Y1 - 2013

M3 - Article

SN - 0141-8955

VL - 36

SP - 961

EP - 966

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - 6

ER -