Rare P
k
phenotype caused by a novel frameshift mutation in B3GALNT1
Transfus Med
.
2023 Apr;33(2):179-180.
doi: 10.1111/tme.12895.
Epub 2022 Jul 14.
Authors
Ling Ma
1
,
Enbo Wang
2
,
Taixiang Liu
1
,
Chengyin Huang
1
,
Wenyi Ding
1
Affiliations
1
Department of Transfusion Research, Jiangsu Province Blood Center, Nanjing, China.
2
Department of Transfusion Medicine, The First People's Hospital of Lianyungang, Lianyungang, China.
PMID:
35836312
DOI:
10.1111/tme.12895
No abstract available
Publication types
Letter
MeSH terms
Frameshift Mutation*
Humans
Phenotype