Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one allele (Q42282561)
scientific article published on January 1994
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(P31) (Q13442814)
(P50) (Q7598948)
(Q30505810)
(P304) 169-184
(P407) (Q1860)
(P433) 2
(P478) 17
(P577) Saturday, January 1, 1994
(P921) (Q750826)
(Q124059385)
(P1433) (Q6295359)
(P1476) "Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one allele" (language: en)
(P2093) N Gregersen
V Winter
J M Saudubray
U Wendel
T G Jensen
S Kølvraa
W Lehnert
L Bolund
(P2860) (Q54649637)
(Q41598951)
(Q41888206)
(Q24316978)
(Q71848169)
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(Q34164301)
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(Q61763893)
(Q68137536)
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(Q37004290)
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(Q54337873)
(Q48213833)
(Q67888318)
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other details
description scientific article published on January 1994

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