Pertti Aula

Distribution of cytoplasmic vacuoles in blood T and B lymphocytes in two lysosomal disorders

J. Rapola, L. Andersson, P. Aula, 1975, Virchows Archiv. B, Cell pathology.

Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantation

C. Greenberg, P. Aula, L. Seargeant, 1997, Clinical genetics.

Characterization of a mannose‐containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU)

P. Aula, K. Sugahara, I. Yamashina, 1976, FEBS letters.

mtDNA Haplotype Analysis in Finnish Families with Leber Hereditary Optic Neuroretinopathy

P. Sistonen, K. Huoponen, M. Savontaus, 1997, European journal of human genetics : EJHG.

Mutations in subunit 6 of the F1F0‐ATP synthase cause two entirely different diseases

M. Wikström, M. Savontaus, A. Majander, 1997, FEBS letters.