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A null-mutated lysyl hydroxylase gene in a compound heterozygote British patient with Ehlers-Danlos syndrome type VI
Jari Heikkinen, Birgitta Pousi, Michael Pope, Raili MyllyläVolume:
14
Year:
1999
Language:
english
Pages:
1
DOI:
10.1002/(sici)1098-1004(199910)14:43.0.co;2-p
File:
PDF, 216 KB
english, 1999