A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction.
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A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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2011年论文
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name
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@en
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@nl
type
label
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@en
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@nl
prefLabel
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@en
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@nl
P2093
P2860
P356
P1476
A Patient with Congenital Gene ...... ary Mitochondrial Dysfunction.
@en
P2093
Ellen H Jeninga
Eric Kalkhoven
Johannes M P J Breur
Monique de Vroede
Nanda M Verhoeven-Duif
Nicole Hamers
Ruud Berger
P2860
P356
10.1007/8904_2011_86
P577
2011-11-04T00:00:00Z