Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood (DOI:10.1016/j.ajhg.2008.09.002)

Avraham Zeharia; Avraham Shaag; Riekelt H. Houtkooper; Tareq Hindi; Pascale de Lonlay; Gilli Erez; Laurence Hubert; Ann Saada; Yves de Keyzer; Gideon Eshel; Frédéric M. Vaz; Ophry Pines; Orly Elpeleg

doi:https://doi.org/10.1016/j.ajhg.2008.12.003

Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood (DOI:10.1016/j.ajhg.2008.09.002)

Avraham Zeharia, Avraham Shaag, Riekelt H. Houtkooper, Tareq Hindi, Pascale de Lonlay, Gilli Erez, Laurence Hubert, Ann Saada, Yves de Keyzer, Gideon Eshel, Frédéric M. Vaz, Ophry Pines, Orly Elpeleg

Amsterdam Gastroenterology Endocrinology Metabolism (AMC)

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Original language	English
Pages (from-to)	95
Number of pages	1
Journal	American journal of human genetics
Volume	84
Issue number	1
DOIs	https://doi.org/10.1016/j.ajhg.2008.12.003
Publication status	Published - 9 Jan 2009

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https://doi.org/10.1016/j.ajhg.2008.12.003

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@article{55a38012747d4d4ea62cd860d8aad29e,

title = "Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood (DOI:10.1016/j.ajhg.2008.09.002)",

author = "Avraham Zeharia and Avraham Shaag and Houtkooper, {Riekelt H.} and Tareq Hindi and {de Lonlay}, Pascale and Gilli Erez and Laurence Hubert and Ann Saada and {de Keyzer}, Yves and Gideon Eshel and Vaz, {Fr{\'e}d{\'e}ric M.} and Ophry Pines and Orly Elpeleg",

year = "2009",

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doi = "https://doi.org/10.1016/j.ajhg.2008.12.003",

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T1 - Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood (DOI:10.1016/j.ajhg.2008.09.002)

AU - Zeharia, Avraham

AU - Shaag, Avraham

AU - Houtkooper, Riekelt H.

AU - Hindi, Tareq

AU - de Lonlay, Pascale

AU - Erez, Gilli

AU - Hubert, Laurence

AU - Saada, Ann

AU - de Keyzer, Yves

AU - Eshel, Gideon

AU - Vaz, Frédéric M.

AU - Pines, Ophry

AU - Elpeleg, Orly

PY - 2009/1/9

Y1 - 2009/1/9

UR - http://www.scopus.com/inward/record.url?scp=58149103028&partnerID=8YFLogxK

U2 - https://doi.org/10.1016/j.ajhg.2008.12.003

DO - https://doi.org/10.1016/j.ajhg.2008.12.003

M3 - Comment/Letter to the editor

SN - 0002-9297

VL - 84

SP - 95

JO - American journal of human genetics

JF - American journal of human genetics

IS - 1

ER -

Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood (DOI:10.1016/j.ajhg.2008.09.002)

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