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Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).
Eur J Hum Genet. 2002 Feb;10(2):91-4. doi: 10.1038/sj.ejhg.5200743.
Eur J Hum Genet. 2002.
PMID: 11938437
Prenatal diagnosis of Ullrich congenital muscular dystrophy using haplotype analysis and collagen VI immunocytochemistry.
Brockington M, Brown SC, Lampe A, Yuva Y, Feng L, Jimenez-Mallebrera C, Sewry CA, Flanigan KM, Bushby K, Muntoni F.
Brockington M, et al.
Prenat Diagn. 2004 Jun;24(6):440-4. doi: 10.1002/pd.902.
Prenat Diagn. 2004.
PMID: 15229843
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