Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis

Publisher: John Wiley & Sons Inc

E-ISSN: 1399-0004|88|1|95-97

ISSN: 0009-9163

Source: CLINICAL GENETICS, Vol.88, Iss.1, 2015-07, pp. : 95-97

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