Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.
about
Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiencyMain clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability.Dystrophin in the nervous system.
P2860
Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.
description
1994 nî lūn-bûn
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1994年の論文
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1994年学术文章
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name
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@en
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@nl
type
label
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@en
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@nl
prefLabel
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@en
Assessment of the 50-kDa dystr ...... recessive muscular dystrophy.
@nl
P2093
P50
P1476
Assessment of the 50-kDa dystr ...... l recessive muscular dystrophy
@en
P2093
K Matsumura
M R Passos-Bueno
R C Pavanello
P304
P356
10.1016/0022-510X(94)90213-5
P577
1994-05-01T00:00:00Z