the study reports the distribution analysis of the SCA17 repeat in 98 sporadic Italian HDL patients not carrying pathogenic expansions in the huntingtin and junctophilin-3 genes.
Common phenotypes in Huntington’s disease like and spinocerebellar ataxia type 17 patients / P. Forleo; E. Cellini; B. Nacmias; A. Tedde; Silvia Bagnoli; Silvia Piacentini; Sandro Sorbi. - In: ANNALS OF NEUROLOGY. - ISSN 1531-8249. - STAMPA. - 55(6):(2004), pp. 1-2.
Common phenotypes in Huntington’s disease like and spinocerebellar ataxia type 17 patients
NACMIAS, BENEDETTA;TEDDE, ANDREA;BAGNOLI, SILVIA;PIACENTINI, SILVIA;SORBI, SANDRO
2004
Abstract
the study reports the distribution analysis of the SCA17 repeat in 98 sporadic Italian HDL patients not carrying pathogenic expansions in the huntingtin and junctophilin-3 genes.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
