Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome (Q42605402)
scientific article published on August 1999
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Current Data About Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome
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(P1476) "Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome" (language: en)
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Y H Jiang
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J Bressler
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D Armstrong
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other details
description scientific article published on August 1999

External Links
(P356) 10.1093/HMG/8.8.1357
(P698) 10400982
(P5875) 12898297