Manifestation of recessive combined D‐2‐, L‐2‐hydroxyglutaric aciduria in combination with 22q11.2 deletion syndrome

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|176|2|351-358

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.176, Iss.2, 2018-02, pp. : 351-358

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Abstract