about
Leigh syndrome associated with a novel mutation in the COX15 gene.First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population.Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro.Hereditary inclusion body myopathy in Persian Jews: a case report from Iran.A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene.A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β.A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities.Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series.Segregation of a novel MLH1 mutation in an Iranian Lynch syndrome familyA new missense mutation in the BCKDHB gene causes the classic form of maple syrup urine disease (MSUD)
P50
Q34517478-8077A39D-A66B-4DD5-A562-C73AAD839F9BQ36887315-BADAC170-BC55-49F0-A117-EF811308981DQ39038023-DD01C571-B8B6-47F9-880A-94CD8E3B456AQ43689096-FC32EDA6-D6AA-47E5-8658-255D310BA0C7Q43702973-4B9BF54C-35EB-435A-B5DD-6A3C1F7B0BA1Q50512865-0AA48633-B8B4-4C6D-A3B9-AEFC3112B855Q50568405-B48C6345-9C30-4526-920F-1A8B4979CE19Q53095042-A10FA002-2253-45C2-96AB-53FE491B9EF1Q85544879-B5CB4CF3-1514-4475-8C2B-917CEC06D4F5Q85932847-782B0F77-8226-4B85-B219-26CB1A5E78ED
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Mohammad Miryounesi
@en
Mohammad Miryounesi
@nl
type
label
Mohammad Miryounesi
@en
Mohammad Miryounesi
@nl
prefLabel
Mohammad Miryounesi
@en
Mohammad Miryounesi
@nl
P31
P496
0000-0003-4705-3794