Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
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Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient.
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2016 nî lūn-bûn
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2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
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2016年论文
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2016年论文
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name
Whole Exome Sequencing Reveals ...... an Iranian Pediatric Patient.
@en
type
label
Whole Exome Sequencing Reveals ...... an Iranian Pediatric Patient.
@en
prefLabel
Whole Exome Sequencing Reveals ...... an Iranian Pediatric Patient.
@en
P2093
P2860
P356
P1476
Whole Exome Sequencing Reveals ...... n an Iranian Pediatric Patient
@en
P2093
Mohammad Ghofrani
Mohammad Keramatipour
Mohammad Reza Alaei
Mohsen Taghizadeh
Saeed Talebi
P2860
P304
P356
10.22045/IBJ.2016.07
P577
2016-07-25T00:00:00Z