Identification of Disease-Causing Mutations by Functional Complementation of Patient-Derived Fibroblast Cell Lines.
about
The functional genomics laboratory: functional validation of genetic variants.NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy.Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy
P2860
Identification of Disease-Causing Mutations by Functional Complementation of Patient-Derived Fibroblast Cell Lines.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Identification of Disease-Caus ...... Derived Fibroblast Cell Lines.
@en
type
label
Identification of Disease-Caus ...... Derived Fibroblast Cell Lines.
@en
prefLabel
Identification of Disease-Caus ...... Derived Fibroblast Cell Lines.
@en
P2860
P1476
Identification of Disease-Caus ...... Derived Fibroblast Cell Lines.
@en
P2093
Laura S Kremer
P2860
P304
P356
10.1007/978-1-4939-6824-4_24
P407
P577
2017-01-01T00:00:00Z