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Srinivas Kovvali
Srinivas Kovvali
Item
http://www.wikidata.org/entity/Q87628795
Q87628795
about
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P50
Q47708439-10B063F8-1C9A-4E22-83E2-FB00BF4F0A3B
P50
Srinivas Kovvali
Item
http://www.wikidata.org/entity/Q87628795
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Srinivas Kovvali
@en
Srinivas Kovvali
@nl
type
Item
label
Srinivas Kovvali
@en
Srinivas Kovvali
@nl
prefLabel
Srinivas Kovvali
@en
Srinivas Kovvali
@nl
P31
Q87628795-43FD2FF9-4CD6-4F30-92AA-EE04011B2D0D
P496
Q87628795-5EC197AE-7862-4A97-910C-2CA208C04679
P496
0000-0003-1693-5620
P31
Afgan
P496
0000-0003-1693-5620
http://www.w3.org/2001/XMLSchema#string