Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

Katta Mohan Girisha; Saadi Abdul Vahab; Ashwin B. Dalal; P. M. Gopinath; K. Satyamoorthy

doi:10.1007/s00277-009-0827-2

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

Katta Mohan Girisha, Saadi Abdul Vahab, Ashwin B. Dalal, P. M. Gopinath, K. Satyamoorthy

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	625-626
Number of pages	2
Journal	Annals of Hematology
Volume	89
Issue number	6
DOIs	https://doi.org/10.1007/s00277-009-0827-2
Publication status	Published - 06-2010

All Science Journal Classification (ASJC) codes

General Medicine
Hematology

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10.1007/s00277-009-0827-2

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title = "Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis",

author = "Girisha, {Katta Mohan} and Vahab, {Saadi Abdul} and Dalal, {Ashwin B.} and Gopinath, {P. M.} and K. Satyamoorthy",

year = "2010",

month = jun,

doi = "10.1007/s00277-009-0827-2",

language = "English",

volume = "89",

pages = "625--626",

journal = "Annals of Hematology",

issn = "0939-5555",

publisher = "Springer Science and Business Media Deutschland GmbH",

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TY - JOUR

T1 - Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

AU - Girisha, Katta Mohan

AU - Vahab, Saadi Abdul

AU - Dalal, Ashwin B.

AU - Gopinath, P. M.

AU - Satyamoorthy, K.

PY - 2010/6

Y1 - 2010/6

UR - http://www.scopus.com/inward/record.url?scp=77951626245&partnerID=8YFLogxK

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U2 - 10.1007/s00277-009-0827-2

DO - 10.1007/s00277-009-0827-2

M3 - Letter

C2 - 19727721

AN - SCOPUS:77951626245

SN - 0939-5555

VL - 89

SP - 625

EP - 626

JO - Annals of Hematology

JF - Annals of Hematology

IS - 6

ER -

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

All Science Journal Classification (ASJC) codes

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