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X‐linked creatine transporter defect: A report on two unrelated boys with a severe clinical phenotype
Author(s) -
Anselm I. A.,
Alkuraya F. S.,
Salomons G. S.,
Jakobs C.,
Fulton A. B.,
Mazumdar M.,
Rivkin M.,
Frye R.,
Poussaint T. Young,
Marsden D.
Publication year - 2006
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-006-9997-4
Subject(s) - medical school , medicine , pediatrics , neurology , family medicine , gerontology , psychiatry , medical education
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