Report for Loddo S

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References (2)

Title : Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1 -
Author(s) : Travaglini L , Aiello C , Alesi V , Loddo S , Novelli A , Tozzi G , Bertini E , Leuzzi V , Brancati F
Ref : Brain Dev , 39 :182 , 2017
PubMedID: 27639779

Title : A novel LIPE nonsense mutation found using exome sequencing in siblings with late-onset familial partial lipodystrophy - Farhan_2014_Can.J.Cardiol_30_1649
Author(s) : Farhan SM , Robinson JF , McIntyre AD , Marrosu MG , Ticca AF , Loddo S , Carboni N , Brancati F , Hegele RA
Ref : Can J Cardiol , 30 :1649 , 2014
Abstract : Farhan_2014_Can.J.Cardiol_30_1649
ESTHER : Farhan_2014_Can.J.Cardiol_30_1649
PubMedSearch : Farhan_2014_Can.J.Cardiol_30_1649
PubMedID: 25475467
Gene_locus related to this paper: human-LIPE