Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay

Saskia Koene; Leo A.J. Kluijtmans; Ron Wevers; Donald Mock; Marcel Pasch; Eva Morava

doi:10.1097/MCD.0b013e3282fe99c4

Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay

Saskia Koene, Leo A.J. Kluijtmans, Ron Wevers, Donald Mock, Marcel Pasch, Eva Morava

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

Original language	English
Pages (from-to)	195-198
Number of pages	4
Journal	Clinical Dysmorphology
Volume	17
Issue number	3
DOIs	https://doi.org/10.1097/MCD.0b013e3282fe99c4
State	Published - Jul 2008
Externally published	Yes

Access to Document

10.1097/MCD.0b013e3282fe99c4

Cite this

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title = "Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay",

author = "Saskia Koene and Kluijtmans, {Leo A.J.} and Ron Wevers and Donald Mock and Marcel Pasch and Eva Morava",

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AU - Koene, Saskia

AU - Kluijtmans, Leo A.J.

AU - Wevers, Ron

AU - Mock, Donald

AU - Pasch, Marcel

AU - Morava, Eva

PY - 2008/7

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AN - SCOPUS:51449119083

SN - 0962-8827

VL - 17

SP - 195

EP - 198

JO - Clinical Dysmorphology

JF - Clinical Dysmorphology

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