Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients
2000 ◽
Vol 37
(8)
◽
pp. 579-580
◽
2017 ◽
Vol 21
◽
pp. e139-e140
2013 ◽
Vol 22
(4)
◽
pp. 444-444
◽