Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-deficient Niemann-Pick disease

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2013

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Mutación en SMPD1 en pacientes con deficiencia de esfingomielinaza ácida para Niemann Pick http://t.co/55xv0P7U #ENARM #OpenAccess

Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-... http://t.co/AaIXq8HV

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