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: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

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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10.1016/j.ajhg.2008.12.003

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@article{599d6fb528f4478c9fde344ef538a62e,

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",

month = jan,

day = "9",

doi = "10.1016/j.ajhg.2008.12.003",

language = "English",

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TY - JOUR

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 - https://www.scopus.com/pages/publications/58149103028

U2 - 10.1016/j.ajhg.2008.12.003

DO - 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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