Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain

scientific article published in May 1997

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S0960-8966(97)00425-2
P698PubMed publication ID9185180

P50authorFrancesco MuntoniQ29645259
P2093author name stringDubowitz V
Sewry CA
Bruno S
Wilson LA
Sorokin L
D'Alessandro M
Naom I
P433issue3
P921main subjectcongenital muscular dystrophyQ1321884
phenotypeQ104053
P304page(s)169-175
P577publication date1997-05-01
P1433published inNeuromuscular DisordersQ1981326
P1476titleVariable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain
P478volume7

Reverse relations

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