Počet záznamov: 1
mukopolysacharidózy
SYS d009083 LBL 00000nx--j22000003--45-- 005 20240119195822.2 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a mukopolysacharidózy $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 92; was MUCOPOLYSACCHARIDOSIS 1974-91 $8 eng 330 1-
$a Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. $8 eng 686 $a C16.320.565.202.715 686 $a C16.320.565.595.600 686 $a C17.300.550.575 686 $a C18.452.648.202.715 686 $a C18.452.648.595.600 750 $a Mucopolysaccharidoses $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20070706 820 $a lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES $8 eng 980 $x M
Počet záznamov: 1