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AGC1 deficiency and cerebral hypomyelination.

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AGC1 deficiency and cerebral hypomyelination. / Wolf, Nicole I; Knaap, van der; Marjo, S.

In: NEW ENGL J MED, Vol. 361, No. 20, 20, 2009, p. 1997-1998.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Wolf, NI, Knaap, VD & Marjo, S 2009, 'AGC1 deficiency and cerebral hypomyelination.', NEW ENGL J MED, vol. 361, no. 20, 20, pp. 1997-1998. <http://www.ncbi.nlm.nih.gov/pubmed/19907050?dopt=Citation>

APA

Wolf, N. I., Knaap, V. D., & Marjo, S. (2009). AGC1 deficiency and cerebral hypomyelination. NEW ENGL J MED, 361(20), 1997-1998. [20]. http://www.ncbi.nlm.nih.gov/pubmed/19907050?dopt=Citation

Vancouver

Wolf NI, Knaap VD, Marjo S. AGC1 deficiency and cerebral hypomyelination. NEW ENGL J MED. 2009;361(20):1997-1998. 20.

Bibtex

@article{a6a8eb5118c341faaa86803726d97443,
title = "AGC1 deficiency and cerebral hypomyelination.",
keywords = "Humans, Magnetic Resonance Imaging, Amino Acid Transport Systems, Acidic deficiency, Antiporters deficiency, Atrophy, Cerebrum pathology, Epilepsy, Hereditary Central Nervous System Demyelinating Diseases genetics, Mitochondrial Membrane Transport Proteins genetics, Humans, Magnetic Resonance Imaging, Amino Acid Transport Systems, Acidic deficiency, Antiporters deficiency, Atrophy, Cerebrum pathology, Epilepsy, Hereditary Central Nervous System Demyelinating Diseases genetics, Mitochondrial Membrane Transport Proteins genetics",
author = "Wolf, {Nicole I} and Knaap, {van der} and S Marjo",
year = "2009",
language = "Deutsch",
volume = "361",
pages = "1997--1998",
journal = "NEW ENGL J MED",
issn = "0028-4793",
publisher = "Massachussetts Medical Society",
number = "20",

}

RIS

TY - JOUR

T1 - AGC1 deficiency and cerebral hypomyelination.

AU - Wolf, Nicole I

AU - Knaap, van der

AU - Marjo, S

PY - 2009

Y1 - 2009

KW - Humans

KW - Magnetic Resonance Imaging

KW - Amino Acid Transport Systems, Acidic deficiency

KW - Antiporters deficiency

KW - Atrophy

KW - Cerebrum pathology

KW - Epilepsy

KW - Hereditary Central Nervous System Demyelinating Diseases genetics

KW - Mitochondrial Membrane Transport Proteins genetics

KW - Humans

KW - Magnetic Resonance Imaging

KW - Amino Acid Transport Systems, Acidic deficiency

KW - Antiporters deficiency

KW - Atrophy

KW - Cerebrum pathology

KW - Epilepsy

KW - Hereditary Central Nervous System Demyelinating Diseases genetics

KW - Mitochondrial Membrane Transport Proteins genetics

M3 - SCORING: Zeitschriftenaufsatz

VL - 361

SP - 1997

EP - 1998

JO - NEW ENGL J MED

JF - NEW ENGL J MED

SN - 0028-4793

IS - 20

M1 - 20

ER -