Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients (Q24681036)
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Current Data About Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients
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(P1476) "Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients" (language: en)

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G Hetet
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A Barnier
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T Dupré
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P de Lonlay
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G Durand
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(P854) https://pubmed.ncbi.nlm.nih.gov/10922383
(P813) Saturday, December 12, 2020
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External Links
(P356) 10.1136/JMG.37.8.579
(P698) 10922383
(P932) 1734666
(P5875) 12398350