(Q42484508)
Statements
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Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence (English)
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Vailly J
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Pulkkinen L
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Miquel C
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Christiano AM
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Gerecke D
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Burgeson RE
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Uitto J
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Ortonne JP
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1 April 1995
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104
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4
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462-466
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Identifiers
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