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METHYLMALONIC ACIDURIA, mut(0) TYPE

MedGen UID:
381562
•Concept ID:
C1855115
•
Disease or Syndrome
Synonym: Methylmalonic Aciduria, mut(0) Type
 
OMIM®: 251000; 609058

Recent clinical studies

Diagnosis

Genetic diagnosis of one family with incomplete clinical data.
Xu S, Bhajoo SH, Jiang W
J Pediatr Endocrinol Metab 2013;26(9-10):903-8. doi: 10.1515/jpem-2013-0032. PMID: 23729607

Prognosis

Genetic diagnosis of one family with incomplete clinical data.
Xu S, Bhajoo SH, Jiang W
J Pediatr Endocrinol Metab 2013;26(9-10):903-8. doi: 10.1515/jpem-2013-0032. PMID: 23729607

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