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Details on Person Jassal, B, 2012-06-14

Class:IdInstanceEdit:2318591
_displayNameJassal, B, 2012-06-14
_timestamp2012-06-14 11:34:12
author[Person:73447] Jassal, Bijay
dateTime2012-06-14 15:33:08
(authored)[FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens]
[FailedReaction:9036077] Defective HYAL1 does not hydrolyse (HA)50 [Homo sapiens]
(created)[Person:2318583] Sims, K B
[EntityWithAccessionedSequence:2318584] GUSB R216W [lysosomal lumen] [Homo sapiens]
[FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens]
[Person:2318586] Triggs-Raine, B
[Person:2318587] Dickersin, G R
[Person:2318588] Short, M P
[EntityWithAccessionedSequence:2318589] HYAL1 E268K [lysosomal lumen] [Homo sapiens]
[EntityFunctionalStatus:2318590] loss_of_function of HYAL1 mutants [lysosomal lumen]
[LiteratureReference:2318592] Clinical and biochemical manifestations of hyaluronidase deficiency
[Person:2318593] Rosenberg, A E
List all 24 refering instances
(edited)[FailedReaction:2318585] Defective HYAL1 does not hydrolyse Chondroitin chains [Homo sapiens]
[FailedReaction:9036077] Defective HYAL1 does not hydrolyse (HA)50 [Homo sapiens]
(modified)[Reaction:1793209] HYAL1-4 hydrolyze chondroitin chains [Homo sapiens]
[Pathway:2206280] MPS IX - Natowicz syndrome (Hyaluronan metabolism) [Homo sapiens]
[Pathway:2206281] Mucopolysaccharidoses [Homo sapiens]
[Pathway:2206282] MPS IIIB - Sanfilippo syndrome B [Homo sapiens]
[Pathway:2206285] MPS VI - Maroteaux-Lamy syndrome [Homo sapiens]
[Summation:2206289] Mucopolysaccharidosis II (MPS II, Hunter syndrome, MIM:30990...
[Pathway:2206290] MPS IV - Morquio syndrome A [Homo sapiens]
[Pathway:2206291] MPS IIIC - Sanfilippo syndrome C [Homo sapiens]
[Pathway:2206292] MPS VII - Sly syndrome (Hyaluronan metabolism) [Homo sapiens]
[Summation:2206295] Absence of alpha-L-iduronidase (IDUA, MIM:252800), the enzym...
List all 93 refering instances
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No pathways have been reviewed or authored by Jassal, B, 2012-06-14 (2318591)